UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
 FORM 10-Q

x	QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934	

 For the quarterly period ended: June 30, 2016 
 Or

o	TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934	
 
For the transition period from:              to
 
Commission File No.: 0-19974
 ICU MEDICAL, INC.
(Exact name of Registrant as specified in its charter)

 	 	 	
Delaware	 	33-0022692	
(State or other jurisdiction of	 	(I.R.S. Employer	
incorporation or organization)	 	Identification No.)	

 	 	 	
951 Calle Amanecer, San Clemente, California	 	92673	
(Address of principal executive offices)	 	(Zip Code)	
 (949) 366-2183
(Registrant’s telephone number including area code)
 
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.  Yes  x   No  o
 
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).  Yes  x   No  o
 
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer”, “accelerated filer” and “smaller reporting company” in Rule 12b-2 of the Exchange Act (check one):

 	 	 	
Large accelerated filer x	 	Accelerated filer o	
 	 	 	
Non-accelerated filer o	 	Smaller reporting company o	
(Do not check if a smaller reporting company)	 	 	
 
Indicate the number of shares outstanding of each of the issuer’s classes of common stock, as of the latest practicable date:

 	 	 	
Class	 	Outstanding at July 31, 2016	
Common	 	16,132,041	
 Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act):  Yes o No x

 	

ICU MEDICAL, INC. AND SUBSIDIARIES
Form 10-Q
June 30, 2016

Table of Contents	
 	 	 	 	
PART I.	Financial Information	 	Page Number	
 	 	 	 	
Item 1.	Financial Statements (Unaudited)	 	 	
 	 	 	 	
 	Condensed Consolidated Balance Sheets, at June 30, 2016 and December 31, 2015	 	3	
 	 	 	 	
 	Condensed Consolidated Statements of Income for the Three and Six Months Ended June 30, 2016 and 2015	 	4	
 	 	 	 	
 	Condensed Consolidated Statements of Comprehensive Income for the Three and Six Months Ended June 30, 2016 and 2015	 	5	
 	Condensed Consolidated Statements of Cash Flows for the Six Months Ended June 30, 2016 and 2015	 	6	
 	 	 	 	
 	Notes to Condensed Consolidated Financial Statements	 	7	
 	 	 	 	
Item 2.	Management’s Discussion and Analysis of Financial Condition and Results of Operations	 	14	
 	 	 	 	
Item 3.	Quantitative and Qualitative Disclosures About Market Risk	 	24	
 	 	 	 	
Item 4.	Controls and Procedures	 	24	
 	 	 	 	
PART II.	Other Information	 	 	
Item 1.	Legal Proceedings	 	25	
 	 	 	 	
Item1A.	Risk Factors	 	25	
 	 	 	 	
Item 2.	Unregistered Sales of Equity Securities and Use of Proceeds	 	25	
 	 	 	 	
Item 6.	Exhibits	 	26	
 	 	 	 	
 	Signature	 	27	

2

PART I - FINANCIAL INFORMATION
 	 	
Item1.	Financial Statements (Unaudited)	

ICU MEDICAL, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED BALANCE SHEETS
(In thousands, except par value data)

 	 	 	 	 	 	 	 	
 	June 30,
2016	 	December 31,
2015	
 	(Unaudited)	 	(1)	
ASSETS	 	 	 	
CURRENT ASSETS:	 	

Cash and cash equivalents	$	372,895	
 	 	$	336,164	
 	
Investment securities	27,720	
 	 	41,233	
 	
TOTAL CASH, CASH EQUIVALENTS AND INVESTMENT SECURITIES	400,615	
 	 	377,397	
 	
Accounts receivable, net of allowance for doubtful accounts of $1,114 at June 30, 2016 and $1,101 at December 31, 2015	60,487	
 	 	57,847	
 	
Inventories	49,919	
 	 	43,632	
 	
Prepaid income taxes	12,072	
 	 	14,366	
 	
Prepaid expenses and other current assets	8,092	
 	 	7,631	
 	
Assets held-for-sale	4,209	
 	 	4,134	
 	
TOTAL CURRENT ASSETS	535,394	
 	 	505,007	

PROPERTY AND EQUIPMENT, net	79,704	
 	 	74,320	
 	
GOODWILL	6,245	
 	 	6,463	
 	
INTANGIBLE ASSETS, net	23,183	
 	 	23,936	
 	
DEFERRED INCOME TAXES	18,853	
 	 	17,099	
 	
TOTAL ASSETS	$	663,379	
 	 	$	626,825	

LIABILITIES AND STOCKHOLDERS’ EQUITY	 	

CURRENT LIABILITIES:	 	

Accounts payable	$	18,853	
 	 	$	13,670	
 	
Accrued liabilities	21,759	
 	 	28,948	
 	
TOTAL CURRENT LIABILITIES	40,612	
 	 	42,618	

LONG-TERM LIABILITIES	1,288	
 	 	1,476	
 	
DEFERRED INCOME TAXES	3,764	
 	 	1,372	
 	
INCOME TAX LIABILITY	1,488	
 	 	1,488	
 	
COMMITMENTS AND CONTINGENCIES	—	
 	 	—	
 	
STOCKHOLDERS’ EQUITY:	 	

Convertible preferred stock, $1.00 par value Authorized—500 shares; Issued and outstanding— none	—	
 	 	—	
 	
Common stock, $0.10 par value — Authorized, 80,000 shares; Issued, 16,175 shares at June 30, 2016 and 16,086 shares at December 31, 2015; Outstanding, 16,125 shares at June 30, 2016 and 16,086 shares at December 31, 2015	1,618	
 	 	1,608	
 	
Additional paid-in capital	149,344	
 	 	145,125	
 	
Treasury stock, at cost - 50 shares at June 30, 2016 and 0 shares at December 31, 2015	(4,471	)	 	—	
 	
Retained earnings	488,662	
 	 	453,896	
 	
Accumulated other comprehensive loss	(18,926	)	 	(20,758	)	
TOTAL STOCKHOLDERS' EQUITY	616,227	
 	 	579,871	
 	
TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY	$	663,379	
 	 	$	626,825	
 	
______________________________________________________
(1) December 31, 2015 balances were derived from audited consolidated financial statements.
The accompanying notes are an integral part of these condensed consolidated financial statements.

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ICU MEDICAL, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF INCOME (Unaudited)
(In thousands, except per share data)

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Three months ended June 30,	 	Six months ended June 30,	
 	2016	 	2015	 	2016	 	2015	
REVENUE:	 	

Net sales	$	96,712	
 	 	$	83,662	
 	 	$	186,561	
 	 	$	164,985	
 	
Other	9	
 	 	119	
 	 	15	
 	 	280	
 	
TOTAL REVENUE	96,721	
 	 	83,781	
 	 	186,576	
 	 	165,265	
 	
COST OF GOODS SOLD	46,589	
 	 	40,020	
 	 	87,211	
 	 	78,990	
 	
GROSS PROFIT	50,132	
 	 	43,761	
 	 	99,365	
 	 	86,275	
 	
OPERATING EXPENSES:	 	

Selling, general and administrative	22,491	
 	 	20,318	
 	 	44,466	
 	 	40,492	
 	
Research and development	3,338	
 	 	3,122	
 	 	6,651	
 	 	7,430	
 	
Restructuring and strategic transaction	1,533	
 	 	—	
 	 	1,533	
 	 	—	
 	
Legal settlement	—	
 	 	—	
 	 	—	
 	 	7,059	
 	
TOTAL OPERATING EXPENSES	27,362	
 	 	23,440	
 	 	52,650	
 	 	54,981	
 	
INCOME FROM OPERATIONS	22,770	
 	 	20,321	
 	 	46,715	
 	 	31,294	
 	
BARGAIN PURCHASE GAIN	1,110	
 	 	—	
 	 	1,110	
 	 	—	
 	
OTHER INCOME, net	77	
 	 	240	
 	 	224	
 	 	766	
 	
INCOME BEFORE INCOME TAXES	23,957	
 	 	20,561	
 	 	48,049	
 	 	32,060	
 	
PROVISION FOR INCOME TAXES	(7,351	)	 	(6,991	)	 	(13,283	)	 	(8,804	)	
NET INCOME	$	16,606	
 	 	$	13,570	
 	 	$	34,766	
 	 	$	23,256	
 	
NET INCOME PER SHARE	 	

Basic	$	1.03	
 	 	$	0.86	
 	 	$	2.16	
 	 	$	1.48	
 	
Diluted	$	0.98	
 	 	$	0.83	
 	 	$	2.05	
 	 	$	1.43	
 	
WEIGHTED AVERAGE NUMBER OF SHARES	 	

Basic	16,091	
 	 	15,781	
 	 	16,070	
 	 	15,738	
 	
Diluted	17,000	
 	 	16,352	
 	 	16,964	
 	 	16,302	

The accompanying notes are an integral part of these condensed consolidated financial statements.

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ICU MEDICAL, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME (Unaudited)
(In thousands)

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Three months ended June 30,	 	Six months ended June 30,	
 	2016	
 	2015	 	2016	 	2015	
NET INCOME	$	16,606	
 	 	$	13,570	
 	 	$	34,766	
 	 	$	23,256	
 	
Other comprehensive (loss) income, net of tax of $(746) and $508 for the three months ended June 30, 2016 and 2015, respectively and $413 and $(2,212) for the six months ended June 30, 2016 and 2015, respectively.	 	

Foreign currency translation adjustment	(2,267	)	 	1,868	
 	 	1,832	
 	 	(8,223	)	
TOTAL COMPREHENSIVE INCOME	$	14,339	
 	 	$	15,438	
 	 	$	36,598	
 	 	$	15,033	

The accompanying notes are an integral part of these condensed consolidated financial statements.

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ICU MEDICAL, INC. AND SUBSIDIARIES
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS (Unaudited)
(In thousands)

 	 	 	 	 	 	 	 	
 	Six months ended June 30,	
 	2016	 	2015	
CASH FLOWS FROM OPERATING ACTIVITIES:	 	

Net income	$	34,766	
 	 	$	23,256	
 	
Adjustments to reconcile net income to net cash provided by operating activities:	 	
 	 	 	
Depreciation and amortization	9,648	
 	 	9,026	
 	
Provision for doubtful accounts	—	
 	 	53	
 	
Provision for warranty and returns	(125	)	 	38	
 	
Stock compensation	7,674	
 	 	5,947	
 	
Loss (gain) on disposal of property and equipment	31	
 	 	(33	)	
Bond premium amortization	121	
 	 	1,223	
 	
Bargain purchase gain	(1,110	)	 	—	
 	
Cash provided by (used in) changes in operating assets and liabilities	 	
 	 	 	
Accounts receivable	(2,527	)	 	(5,529	)	
Inventories	(5,479	)	 	(2,267	)	
Prepaid expenses and other assets	(3,784	)	 	(1,375	)	
Accounts payable	3,752	
 	 	1,894	
 	
Accrued liabilities	(5,985	)	 	(1,027	)	
Income taxes, including excess tax benefits and deferred income taxes	4,793	
 	 	(2,031	)	
Net cash provided by operating activities	41,775	
 	 	29,175	
 	
CASH FLOWS FROM INVESTING ACTIVITIES:	 	

Purchases of property and equipment	(9,112	)	 	(5,005	)	
Proceeds from sale of asset	1	
 	 	34	
 	
Business acquisitions, net of cash acquired	(2,606	)	 	—	
 	
Intangible asset additions	(513	)	 	(440	)	
Purchases of investment securities	(18,106	)	 	(17,092	)	
Proceeds from sale of investment securities	31,765	
 	 	49,555	
 	
Net cash provided by investing activities	1,429	
 	 	27,052	
 	
CASH FLOWS FROM FINANCING ACTIVITIES:	 	

Proceeds from exercise of stock options	7,796	
 	 	5,797	
 	
Proceeds from employee stock purchase plan	1,197	
 	 	1,041	
 	
Purchase of treasury stock	(16,911	)	 	(1,435	)	
Net cash (used in) provided by financing activities	(7,918	)	 	5,403	
 	
Effect of exchange rate changes on cash	1,445	
 	 	(6,350	)	
NET INCREASE IN CASH AND CASH EQUIVALENTS	36,731	
 	 	55,280	
 	
CASH AND CASH EQUIVALENTS, beginning of period	336,164	
 	 	275,812	
 	
CASH AND CASH EQUIVALENTS, end of period	$	372,895	
 	 	$	331,092	

NON-CASH INVESTING ACTIVITIES	 	 	 	
  Accounts payable for property and equipment	$	1,574	
 	 	$	232	

The accompanying notes are an integral part of these condensed consolidated financial statements.

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ICU MEDICAL, INC. AND SUBSIDIARIES
NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (Unaudited)

Note 1:	Basis of Presentation	
 
The accompanying unaudited interim condensed consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States of America ("U.S.") and pursuant to the rules and regulations of the Securities and Exchange Commission (“SEC”) and reflect all adjustments, consisting of only normal recurring adjustments, which are, in the opinion of management, necessary for a fair statement of the consolidated results for the interim periods presented. Results for the interim period are not necessarily indicative of results for the full year. Certain information and footnote disclosures normally included in annual consolidated financial statements prepared in accordance with generally accepted accounting principles have been condensed or omitted pursuant to such rules and regulations. The condensed consolidated financial statements should be read in conjunction with the consolidated financial statements and notes thereto included in the Annual Report on Form 10-K of ICU Medical, Inc., a Delaware corporation, filed with the SEC for the year ended December 31, 2015.
 
We operate in one business segment engaged in the development, manufacturing and sale of innovative medical devices used in infusion therapy, critical care and oncology applications.  We sell the majority of our products through our direct sales force and through independent distributors throughout the U. S. and internationally.  Additionally, we sell our products on an original equipment manufacturer basis to other medical device manufacturers. All subsidiaries are wholly owned and are included in the condensed consolidated financial statements.  All intercompany balances and transactions have been eliminated.

Note 2:    New Accounting Pronouncements

Recently Adopted Accounting Standards

In March 2016, the Financial Accounting Standards Board ("FASB") issued Accounting Standard Update ("ASU") No. 2016-09, Compensation - Stock Compensation (Topic 718): Improvements to Employee Share-Based Payment Accounting. The amendments address several aspects of the accounting for share-based payment award transactions, including income tax accounting consequences, classification of awards as either equity or liabilities, and classification on the statement of cash flows. The amendments in this update are effective for annual periods beginning after December 15, 2016. Early adoption is permitted for an entity in any interim or annual period. An entity that elects early adoption must adopt all of the amendments in the same period and any adjustments should be reflected as of the beginning of the fiscal year that includes that interim period. We early adopted this standard during the second quarter ended June 30, 2016. As a result of the adoption, we recognized a $0.8 million and $3.1 million tax benefit as a discrete item during the three and six months ended June 30, 2016, respectively. We elected to retrospectively adopt the presentation of excess tax benefits as an operating activity rather than as a financing activity on the statement of cash flows. Accordingly, the adoption resulted in a $3.1 million and $3.4 million increase in operating cash flows for the periods ended June 30, 2016 and 2015, respectively, and a corresponding $3.1 million and $3.4 million decrease in financing cash flows for the period ended June 30, 2016 and 2015, respectively. We elect to account for forfeitures as they occur.

In September 2015, the FASB issued ASU No. 2015-16, Business Combinations (Topic 805): Simplifying the Accounting for Measurement-Period Adjustments. ASU 2015-16 requires that an acquirer recognize adjustments to provisional amounts that are identified during the measurement period in the reporting period in which the adjustment amounts are determined, including the cumulative effect of the change in provisional amount as if the accounting had been completed at the acquisition date. The adjustments related to previous reporting periods since the acquisition date must be disclosed by income statement line item either on the face of the income statement or in the notes. The amendments are effective prospectively for the fiscal years, and interim reporting periods within those years, beginning on or after December 15, 2015. The adoption of this ASU did not have a material impact on our consolidated financial statements.

In June 2014, the FASB issued ASU No. 2014-12, Compensation - Stock Compensation (Topic 718): Accounting for Share-Based Payments When the Terms of an Award Provide that a Performance Target Could be Achieved after the Requisite Service Period. ASU 2014-12 requires that a performance target that affects vesting, and that could be achieved after the requisite service period, be treated as a performance condition. As such, the performance target should not be reflected in estimating the grant date fair value of the award. This update further clarifies that compensation cost should be recognized in the period in which it becomes probable that the performance target will be achieved and should represent the compensation cost attributable to the period(s) for which the requisite service has already been rendered. The amendments in ASU 2014-12 are effective for annual periods and interim periods within those annual periods beginning after December 15, 2015. Entities

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may apply the amendments in ASU 2014-12 either: (a) prospectively to all awards granted or modified after the effective date; or (b) retrospectively to all awards with performance targets that are outstanding as of the beginning of the earliest annual period presented in the financial statements and to all new or modified awards thereafter. We adopted this ASU on a prospective basis. The adoption did not have a material impact on our consolidated financial statements.

Recently Issued Accounting Standards

In June 2016, the FASB issued ASU 2016-13, Financial Instruments-Credit Losses (Topic 326): Measurement of Credit Losses on Financial Instruments. This update amends the FASB's guidance on the impairment of financial instruments by requiring timelier recording of credit losses on loans and other financial instruments. The ASU adds an impairment model that is based on expected losses rather than incurred losses. The ASU also amends the accounting for credit losses on available-for-sale debt securities and purchased financial assets with credit deterioration. The amendments in this update will be effective for fiscal years beginning after December 15, 2019. Early adoption is permitted as of the fiscal years beginning after December 15, 2018. The updated guidance requires a modified retrospective adoption. We are currently evaluating the impact of this ASU on the consolidated financial statements and related disclosures.

In February 2016, the FASB issued ASU 2016-02, Leases (Topic 842). The amendments in this update require an entity to recognize a right-of-use asset and lease liability for all leases with terms of more than 12 months. Recognition, measurement and presentation of expenses will depend on classification as finance or operating lease. The amendments also require certain quantitative and qualitative disclosures about leasing arrangements. The amendments in this update will be effective for fiscal years beginning after December 15, 2019. Early adoption is permitted. The updated guidance requires a modified retrospective adoption. We are currently evaluating the impact of this ASU on the consolidated financial statements and related disclosures.

In January 2016, the FASB issued ASU 2016-01, Financial Instruments – Overall (Subtopic 825-10): Recognition and Measurement of Financial Assets and Financial Liabilities, which amends certain aspects of recognition, measurement, presentation and disclosure of financial instruments. This amendment requires all equity investments to be measured at fair value with changes in the fair value recognized through net income (other than those accounted for under the equity method of accounting or those that result in the consolidation of the investee). The amendments in this update will be effective for fiscal years beginning after December 15, 2017. Early adoption of the amendments is not permitted with the exception of the provision requiring the recognition in other comprehensive income the fair value change from instrument-specific credit risk measured using the fair value option for financial instruments. We are currently evaluating the impact of this ASU on the consolidated financial statements and related disclosures.
        
In July 2015, the FASB issued ASU No. 2015-11 Inventory (Topic 330): Simplifying the Measurement of Inventory. ASU 2015-11 changes the measurement of inventory from lower of cost or market to lower of cost and net realizable value. The amendments are effective prospectively for the fiscal years, and interim reporting periods within those years, beginning on or after December 15, 2016. We do not anticipate a material impact on our consolidated financial statements from the adoption of this ASU.

In May 2014, the FASB issued ASU No. 2014-09, Revenue from Contracts with Customers (Topic 606). ASU 2014-09 removes inconsistencies and weaknesses in revenue requirements, provides a more robust framework for addressing revenue issues, improves comparability of revenue recognition practices across entities, industries, jurisdictions and capital markets, provides more useful information to users of financial statements through improved disclosure requirements and simplifies the preparation of financial statements by reducing the number of requirements to which an entity must refer. This guidance requires that an entity depict the consideration by applying a five-step analysis in determining when and how revenue is recognized. The new model will require revenue recognition to depict the transfer of promised goods or services to customers in an amount that reflects the consideration a company expects to receive in exchange for those goods or services. On April 1, 2015, the FASB voted for a one-year deferral of the effective date of the new revenue recognition standard, ASU No. 2014-09.  On July 15, 2015, the FASB affirmed these changes, which requires public entities to apply the amendments in ASU 2014-09 for annual reporting beginning after December 15, 2017. Early adoption is permitted beginning after December 31, 2016, the original effective date in ASU 2014-09. Subsequent to the issuance of this ASU, the FASB issued three amendments: ASU No. 2016-08 which clarifies principal versus agent considerations; ASU No. 2016-10 which clarifies guidance related to identifying performance obligations and licensing implementation; and ASU 2016-12 which provides narrow-scope improvements and practical expedients. All of the amendments have the same effective dates mentioned above. We do not anticipate a material impact on our consolidated financial statements from adoption of any of the above ASUs. We expect to adopt the full retrospective transition method when adopting this ASU.

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Note 3: Restructuring Charges

Restructuring Charges

During the year ended December 31, 2015, we incurred restructuring charges related to: (i) an agreement with Dr. Lopez, a member of our Board of Directors and a former employee in our research and development department, pursuant to which we bought out Dr. Lopez's right to employment under his then-existing employment agreement; (ii) the reorganization of our corporate infrastructure, resulting in one-time employee termination benefits and other associated costs; and (iii) a commitment to a plan to sell our Slovakia manufacturing facility. The assets of the manufacturing facility are classified as assets held for sale and are included as a separate line item in our condensed consolidated balance sheet. The sale is expected to be completed during the second half of 2016. The plan to close the facility resulted in a pre-tax restructuring charge for employee termination benefits, government incentive repayments and other associated costs. There was $0.4 million in restructuring charges incurred for the three and six months ended June 30, 2016. Of these charges $0.2 million were related to the closure of the Slovakian manufacturing facility and are included in the below table, and the other $0.2 million was related to a one-time charge unrelated to the events disclosed above.

The following table summarizes the details of changes in our restructuring-related accrual for the period ending June 30, 2016 (in thousands):

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Accrued Balance December 31, 2015	 	Charges
Incurred	 	Payments	 	Currency
Translation	 	Other Adjustments	 	Accrued Balance
June 30,
 2016	
Severance pay and benefits	$	2,505	
 	 	$	25	
 	 	$	(1,421	)	 	$	69	
 	 	$	172	
 	 	$	1,350	
 	
Government incentive repayment	1,884	
 	 	—	
 	 	(1,769	)	 	57	
 	 	(172	)	 	—	
 	
Employment agreement buyout	1,845	
 	 	—	
 	 	(188	)	 	—	
 	 	—	
 	 	1,657	
 	
Other corporate restructuring	305	
 	 	168	
 	 	(251	)	 	—	
 	 	—	
 	 	222	
 	
 	$	6,539	
 	 	$	193	
 	 	$	(3,629	)	 	$	126	
 	 	$	—	
 	 	$	3,229	

Note 4: Acquisition and Strategic Transaction Expenses

On April 4, 2016, we acquired all of the outstanding shares of Tangent Medical Technologies, Inc. ("Tangent") for $2.6 million in cash. Tangent designs, develops, and commercializes intravenous catheters and associated products for the improvement of infusion therapy. Tangent's products enhance our infusion therapy product offering. As a result of the Tangent acquisition, we immediately recognized a $1.1 million bargain purchase gain that represented the excess of the estimated fair market value of the identifiable tangible and intangible assets acquired, liabilities assumed and deferred tax assets over the total purchase consideration. The bargain purchase was driven by our ability to realize acquired deferred tax assets. The purchase price allocation is subject to further adjustment in order to account for final tax related matters such as filing of final tax return.

We incurred $1.1 million in transaction costs during the three and six months ended June 30, 2016 related to our 2015 acquisition of EXC Holding Corp. and to our second quarter 2016 acquisition of Tangent mentioned above.

Note 5:    Legal Settlements

On April 2, 2015, an arbitrator ruled on a breach of contract claim between us and a customer, Hospira, Inc., awarding Hospira $8.2 million Canadian dollars ($6.5 million U.S. dollars). The arbitrator also ruled that we pay 75% of Hospira's legal fees and expenses, which were $0.7 million U.S. dollars. During the six months ended June 30, 2015, we recorded an estimated total charge of $7.1 million related to the settlement and associated fees, which is presented as a separate line item in our condensed consolidated income statement. These charges were fully paid during the second quarter of 2015.
    
Note 6:    Fair Value Measurement
 
Our investment securities consist of certificates of deposit, corporate bonds, U.S. Treasury securities, commercial paper and federal tax-exempt state and municipal government debt. All investment securities are considered available-for-sale and are “investment grade”, carried at fair value and there have been no gains or losses on their disposal. As of June 30, 2016, we had $3.5 million of our investment securities as Level 1 assets, which are certificates of deposit and U.S. Treasury securities

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with quoted prices in active markets. As of June 30, 2016, we had $24.2 million of our investment securities as Level 2 assets, which are pre-refunded municipal securities, corporate bonds and commercial paper and are valued using observable market based inputs such as quoted prices, interest rates and yield curves.

There were no transfers between Levels during the first half of 2016.

The following tables provide the assets and liabilities carried at fair value measured on a recurring basis for the periods indicated (in thousands):

 	Fair value measurements at June 30, 2016 using	
 	Total carrying
value	 	Quoted prices
in active
markets for
identical
assets (level 1)	 	Significant
other
observable
inputs (level 2)	 	Significant
unobservable
inputs (level 3)	
Available for sale securities	$	27,720	
 	 	$	3,504	
 	 	$	24,216	
 	 	$	—	
 	
 	$	27,720	
 	 	$	3,504	
 	 	$	24,216	
 	 	$	—	

 	
 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Fair value measurements at December 31, 2015 using	
 	Total carrying
value	 	Quoted prices
in active
markets for
identical
assets (level 1)	 	Significant
other
observable
inputs (level 2)	 	Significant
unobservable
inputs (level 3)	
Available for sale securities	$	41,233	
 	 	$	8,785	
 	 	$	32,448	
 	 	$	—	
 	
 	$	41,233	
 	 	$	8,785	
 	 	$	32,448	
 	 	$	—	

In November 2015, our Board of Directors authorized the closure of our Vrable, Slovakia manufacturing facility. As a result of the closure we reclassified the land and building related to the Slovakia facility as held for sale. Our assets held for sale are included as a separate line item in our condensed consolidated balance sheets. The initial fair value of our assets held for sale was estimated using the income approach and is based on critical estimates, judgments and assumptions derived from: analysis of market conditions; building condition; comparable properties; and rental income and expense (Level 3). Subsequent to the initial valuation, we evaluate the carrying value of our assets held for sale when circumstances indicate the carrying value of those assets may or may not be recoverable; there were no such indicators during the period ended June 30, 2016. The increase in our assets held for sale as of June 30, 2016, as compared to December 31, 2015, was due to currency translation.

The following tables provide the assets and liabilities carried at fair value on a non-recurring basis for the periods indicated (in thousands):

 	Fair value measurements at June 30, 2016 using	
 	Total carrying
value	 	Quoted prices
in active
markets for
identical
assets (level 1)	 	Significant
other
observable
inputs (level 2)	 	Significant
unobservable
inputs (level 3)	
Assets held for sale	$	4,209	
 	 	$	—	
 	 	$	—	
 	 	$	4,209	
 	
 	$	4,209	
 	 	$	—	
 	 	$	—	
 	 	$	4,209	

 	
 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Fair value measurements at December 31, 2015 using	
 	Total carrying
value	 	Quoted prices
in active
markets for
identical
assets (level 1)	 	Significant
other
observable
inputs (level 2)	 	Significant
unobservable
inputs (level 3)	
Assets held for sale	$	4,134	
 	 	$	—	
 	 	$	—	
 	 	$	4,134	
 	
 	$	4,134	
 	 	$	—	
 	 	$	—	
 	 	$	4,134	

 

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Note 7: Investment Securities

Our investment securities consist of certificates of deposit, corporate bonds, U.S. Treasury securities, commercial paper and federal tax-exempt state and municipal government debt. All investment securities are considered available-for-sale and are “investment grade”, carried at fair value, and there have been no gains or losses on their disposal. Unrealized gains and losses on available-for-sale securities, net of tax, are included in accumulated other comprehensive loss in the stockholders' equity section of our condensed consolidated balance sheets. We had no gross unrealized gains or losses on available-for-sale securities at June 30, 2016 or December 31, 2015. The scheduled maturities of the debt securities are between 2016 and 2036 and are all callable within one year.
    
The investment securities consist of the following at June 30, 2016 and December 31, 2015 (in thousands):

 	June 30,
2016	 	December 31, 2015	
Federal and municipal tax-exempt debt securities	$	8,143	
 	 	$	4,951	
 	
Corporate bonds	15,374	
 	 	25,400	
 	
U.S. Treasury securities	3,004	
 	 	7,537	
 	
Commercial paper	699	
 	 	2,097	
 	
Certificates of deposit	500	
 	 	1,248	
 	
Total investment securities	$	27,720	
 	 	$	41,233	

Note 8: Inventories
 
Inventories consisted of the following (in thousands):

 	 	 	 	 	 	 	 	
 	June 30,
2016	 	December 31, 2015	
Raw material	$	27,265	
 	 	$	24,681	
 	
Work in process	4,258	
 	 	4,282	
 	
Finished goods	18,396	
 	 	14,669	
 	
Total inventories	$	49,919	
 	 	$	43,632	

Note 9:    Property and Equipment

Property and equipment consisted of the following (in thousands):

 	 	 	 	 	 	 	 	
 	June 30,
2016	 	December 31, 2015	
Machinery and equipment	$	99,259	
 	 	$	96,909	
 	
Land, building and building improvements	60,107	
 	 	56,716	
 	
Molds	37,452	
 	 	36,436	
 	
Computer equipment and software	25,559	
 	 	23,346	
 	
Furniture and fixtures	3,919	
 	 	3,638	
 	
Construction in progress	10,918	
 	 	6,003	
 	
Total property and equipment, cost	237,214	
 	 	223,048	
 	
Accumulated depreciation	(157,510	)	 	(148,728	)	
Property and equipment, net	$	79,704	
 	 	$	74,320	

Note 10:     Net Income Per Share
 
Net income per share is computed by dividing net income by the weighted average number of common shares outstanding. Diluted net income per share is computed by dividing net income by the weighted average number of common shares outstanding plus dilutive securities. Dilutive securities are outstanding common stock options and restricted stock units

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(excluding stock options with an exercise price in excess of the average market value for the period), less the number of shares that could have been purchased with the proceeds from the exercise of the options, using the treasury stock method. Options that are anti-dilutive because their exercise price exceeded the average market price of the common stock for the period approximated 33,000 for the three months ended June 30, 2015 and 4,300 and 16,000 for the six months ended June 30, 2016 and 2015, respectively. There were no anti-dilutive options for the three months ended June 30, 2016.

The following table presents the calculation of net earnings per common share (“EPS”) — basic and diluted (in thousands, except per share data):

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Three months ended June 30,	 	Six months ended June 30,	
 	2016	 	2015	 	2016	 	2015	
Net income	$	16,606	
 	 	$	13,570	
 	 	$	34,766	
 	 	$	23,256	
 	
Weighted average number of common shares outstanding (for basic calculation)	16,091	
 	 	15,781	
 	 	16,070	
 	 	15,738	
 	
Dilutive securities(1)	909	
 	 	571	
 	 	894	
 	 	564	
 	
Weighted average common and common equivalent shares outstanding (for diluted calculation)	17,000	
 	 	16,352	
 	 	16,964	
 	
 	16,302	
 	
EPS — basic	$	1.03	
 	 	$	0.86	
 	 	$	2.16	
 	 	$	1.48	
 	
EPS — diluted	$	0.98	
 	 	$	0.83	
 	 	$	2.05	
 	 	$	1.43	
 	
 ______________________________

(1) During the second quarter of 2016, we early adopted ASU 2016-09, Compensation - Stock Compensation (Topic 718): Improvements to Employee Share-Based Payment Accounting see Note 2, New Accounting Pronouncements, for more detail. Under this ASU, the assumed proceeds from applying the treasury stock method when computing earnings per share no longer includes the amount of excess tax benefits or deficiencies that used to be recognized as additional paid-in capital. This change in the treasury stock method was made on a prospective basis, with adjustments reflected as of the beginning of the 2016 fiscal year. The adoption of this ASU impacted weighted average common and common equivalent shares outstanding by 345,000 shares and 340,000 shares for the three and six months ended June 30, 2016, respectively.

Note 11:     Major Customer
    
We had revenue equal to 10% or more of total revenue from one customer, Hospira, Inc. a subsidiary of Pfizer. Such revenues were 34% and 35% of total revenue for the three months ended June 30, 2016 and 2015, respectively and 34% and 36% of total revenue for the six months ended June 30, 2016 and 2015, respectively. As of June 30, 2016 and December 31, 2015, we had accounts receivable from Pfizer of 35% and 40% of consolidated accounts receivable, respectively.
 
Note 12:     Income Taxes
 
Income taxes were accrued at an estimated effective tax rate of 28% and 27% for the six months ended June 30, 2016 and 2015, respectively. Those rates differ from that computed at the federal statutory rate of 35%.

The effective tax rate for the six months ended June 30, 2016 differs from the federal statutory rate of 35% principally because of the effect of foreign and state income taxes, tax credits, deductions for domestic production activities, and included material discrete tax benefits related to the adoption of ASU 2016-09, see below.
The effective tax rate during the six months ended June 30, 2016 included a material tax benefit of $3.1 million related to the early adoption of ASU 2016-09, Compensation - Stock Compensation (Topic 718): Improvements to Employee Share-Based Payment Accounting, which amends current accounting to now recognize all excess tax benefits and all tax deficiencies as income tax benefit or expense in the reporting period in which they occur. The income tax benefit was treated as a discrete item when determining the annual estimated effective tax rate see Note 2, New Accounting Pronouncements for further detail.
The effective tax rate for the six months ended June 30, 2015 differs from the federal statutory rate principally because of the effect of foreign and state income taxes, tax credits, deductions for domestic production activities and material discrete tax benefits related to the impact of changes in estimates of tax reserves related to uncertainties in income taxes as a result of the favorable conclusion of recent federal and state examinations.

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Note13: Treasury Stock

In July 2010, our Board of Directors approved a common stock purchase plan to purchase up to $40.0 million of our common stock. This plan has no expiration date. For the six months ended June 30, 2016 we purchased 174,885 shares of our common stock for $15.4 million, including commissions. As of June 30, 2016, we had $7.2 million remaining on this purchase plan. We expect to use the treasury stock to issue shares for stock option exercises, restricted stock grants and employee stock purchase plan stock purchases.

Additionally, for the six months ended June 30, 2016, we withheld 17,661 shares of our common stock from employee vested restricted stock units in consideration for $1.6 million in payments made on the employee's behalf for their minimum statutory income tax withholding obligations.
 
Note 14: Commitments and Contingencies

From time to time, we are involved in various legal proceedings, most of which are routine litigation, in the normal course of business.  Our management does not believe that the resolution of the unsettled legal proceedings that we are involved with will have a material adverse impact on our financial position or results of operations.
 
In the normal course of business, we have agreed to indemnify our officers and directors to the maximum extent permitted under Delaware law and to indemnify customers as to certain intellectual property matters or other matters related to sales of our products.  There is no maximum limit on the indemnification that may be required under these agreements.  Although we can provide no assurances, we have never incurred, nor do we expect to incur, any material liability for indemnification.

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Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations
 
The following information should be read in conjunction with the condensed consolidated financial statements and accompanying notes in this Form 10-Q, as well as the audited consolidated financial statements and related notes for the fiscal year ended December 31, 2015 included in our Annual Report on Form 10-K.
    
When used in this report, the terms “we,” “us,” and “our,” refer to ICU Medical, Inc. and its subsidiaries included in our condensed consolidated financial statements unless context requires otherwise.

Business Overview
    
We are a leader in the development, manufacture and sale of innovative medical devices used in infusion therapy, critical care and oncology applications.  Our product line includes needlefree connection devices, custom infusion sets, closed system transfer devices ("CSTD") for the handling of hazardous drugs, advanced sensor catheters, closed blood sampling systems and innovative hemodynamic monitoring systems.

Our products are used in acute care hospitals and ambulatory clinics in more than 60 countries throughout the world.     The following table summarizes our total worldwide revenue by domestic and international markets by amount and as a percentage of total revenue (in millions, except percentages):

 	Three months ended June 30,	 	Six months ended June 30,	 	Fiscal year ended	
 	2016	 	2015	 	2016	 	2015	 	2015	 	2014	
 	$	 	% of Revenue	 	$	 	% of Revenue	 	$	 	% of Revenue	 	$	 	% of Revenue	 	$	 	% of Revenue	 	$	 	% of Revenue	
Domestic	$	69.6	
 	 	72	%	 	$	57.6	
 	 	69	%	 	$	131.3	
 	 	70	%	 	$	115.3	
 	 	70	%	 	$	241.8	
 	 	71	%	 	$	212.6	
 	 	69	%	
International	27.1	
 	 	28	%	 	26.2	
 	 	31	%	 	55.3	
 	 	30	%	 	50.0	
 	 	30	%	 	99.9	
 	 	29	%	 	96.7	
 	 	31	%	
Total Revenue	$	96.7	
 	 	100	%	 	$	83.8	
 	 	100	%	 	$	186.6	
 	 	100	%	 	$	165.3	
 	 	100	%	 	$	341.7	
 	 	100	%	 	$	309.3	
 	 	100	%	

We categorize our products into three main market segments: Infusion Therapy, Critical Care and Oncology. Our primary products include:

Infusion Therapy
•Needlefree connector products
◦MicroClave® and MicroClave Clear
◦Neutron® 
◦NanoClave® 
◦Clave® 
◦SwabCap® 
•Custom infusion sets
•Tego® needlefree hemodialysis connector
    
Critical Care
•Hemodynamic monitoring systems
•Closed Blood Sampling and Conservation Systems
•Other Critical Care Products and Accessories

Oncology
•ChemoLock® CSTD and components
•ChemoClave® CSTD and components
•Diana™ hazardous drug compounding system

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The following table sets forth, for the periods indicated, total revenue by product line as a percentage of total revenue: 

 	 	Three months ended June 30,	 	Six months ended June 30,	 	Fiscal year ended	
Product line	 	2016	 	2015	 	2016	 	2015	 	2015	 	2014	
Infusion therapy	 	73	%	 	69	%	 	73	%	 	71	%	 	72	%	 	70	%	
Critical care	 	14	%	 	18	%	 	14	%	 	17	%	 	16	%	 	18	%	
Oncology	 	13	%	 	13	%	 	13	%	 	12	%	 	12	%	 	12	%	
 	 	100	%	 	100	%	 	100	%	 	100	%	 	100	%	 	100	%	

We currently sell our products through direct channels, which include distributors and the end users of our products and as an original equipment manufacturer ("OEM") supplier. Most of our independent distributors handle the full line of our products.

Our largest customer is Hospira, Inc. a subsidiary of Pfizer, to which we distribute our products as an OEM supplier. Pfizer accounted for 34%, 36% and 36% of our worldwide revenue in the first six months of 2016 and each of the years ended 2015 and 2014, respectively. We began this relationship in 1995 with Hospira, which was acquired by Pfizer in September 2015. Our related agreements extend through December 2018. Our agreements with Pfizer provide them with conditional rights to distribute certain of our Clave family and other products to certain categories of customers both in the United States ("U.S.") and foreign countries. Depending on the product and category of customer, these rights may be exclusive or nonexclusive. Pfizer purchases Clave products both as finished goods end-products for distribution to healthcare providers and in bulk for assembly into Pfizer infusion disposable products. The MicroClave, MicroClave Clear, ChemoClave CSTD and pre-pierced connector products are purchased and packaged separately as finished good end products. We also serve as the exclusive manufacturer for certain custom intravenous products that are sold by the same subsidiary. These products are promoted under the name SetSource. Our relationship with Pfizer has been and will continue to be important for our growth. We expect revenue from infusion therapy products and new product sales to Pfizer to remain a significant percentage of our revenue. An adverse change in our relationship with Pfizer, or a deterioration of Pfizer’s position in the market, could have an adverse effect on us.

We believe that as healthcare providers continue to either consolidate or join major buying organizations, the success of our products will depend, in part, on our ability, either independently or through strategic relationships such as our Pfizer relationship, to secure long-term contracts with large healthcare providers and major buying organizations.  As a result of this marketing and distribution strategy we derive most of our revenue from a relatively small number of distributors and manufacturers.  The loss of a strategic relationship with a customer or a decline in demand for manufacturing customers' products could have a material adverse effect on our operating results.
 
We believe that achievement of our growth objectives worldwide will require increased efforts by us in sales and marketing and product acquisition and development; however, there is no assurance that we will be successful in implementing our growth strategy. Product development or acquisition efforts may not succeed, and even if we do develop or acquire additional products, there is no assurance that we will achieve profitable sales of such products.  Increased expenditures for sales and marketing and product acquisition and development may not yield desired results when expected, or at all.  While we have taken steps to control these risks, there are certain risks that may be outside of our control, and there is no assurance that steps we have taken will succeed.

Seasonality/Quarterly Results
 
The healthcare business in the U.S. is subject to quarterly fluctuations due to frequency of illness during the seasons, elective procedures, and over the last few years, the economy. In Europe, the healthcare business generally slows down in the summer months due to vacations resulting in fewer elective surgeries.  In addition, we can experience fluctuations in net sales as a result of variations in the ordering patterns of our largest customers, which may be driven more by production scheduling and their inventory levels, and less by seasonality.  Our expenses often do not fluctuate in the same manner as net sales, which may cause fluctuations in operating income that are disproportionate to fluctuations in our revenue.

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Acquisition

On April 4, 2016, we acquired all of the outstanding shares of Tangent Medical Technologies, Inc. ("Tangent") for $2.6 million in cash. Tangent designs, develops, and commercializes intravenous catheters and associated products for the improvement of infusion therapy. Tangent's products enhance our infusion therapy product offering. We do not expect any significant commercial results from this product line over the next eighteen to twenty-four months while we make changes to this product.

Consolidated Results of Operations

We present income statement data in Part I, Item 1 - Financial Statements. The following table shows, for the three and six months ended June 30, 2016 and 2015, respectively, and the year ended December 31, 2015, the percentages of each income statement caption in relation to total revenue:

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	 	Three months ended
June 30,	 	Six Months Ended
June 30,	 	Fiscal year ended	
 	 	2016	 	2015	 	2016	 	2015	 	2015	
Total revenue	 	100	%	 	100	%	 	100	%	 	100	%	 	100	%	
Gross margin	 	52	%	 	52	%	 	53	%	 	52	%	 	53	%	
Selling, general and administrative expenses	 	23	%	 	24	%	 	24	%	 	25	%	 	24	%	
Research and development expenses	 	3	%	 	4	%	 	3	%	 	4	%	 	5	%	
Restructuring and strategic transaction	 	2	%	 	—	%	 	1	%	 	—	%	 	2	%	
Legal settlements	 	—	%	 	—	%	 	—	%	 	4	%	 	1	%	
Impairment of assets held for sale	 	—	%	 	—	%	 	—	%	 	—	%	 	1	%	
Total operating expenses	 	28	%	 	28	%	
 	28	%	
 	33	%	
 	33	%	
Income from operations	 	24	%	 	24	%	 	25	%	 	19	%	 	20	%	
Bargain purchase gain	 	1	%	 	—	%	 	1	%	 	—	%	 	—	%	
Other income, net	 	—	%	 	—	%	 	—	%	 	—	%	 	—	%	
Income before income taxes	 	25	%	 	24	%	 	26	%	 	19	%	 	20	%	
Income taxes	 	8	%	 	8	%	 	7	%	 	5	%	 	7	%	
Net income	 	17	%	 	16	%	 	19	%	 	14	%	 	13	%	
    
Infusion Therapy Revenue

The following table summarizes our total infusion therapy revenue by direct and OEM distribution channels (in millions):

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Three months ended June 30,	 	Six months ended June 30,	
 	2016	 	2015	 	$ Change	 	% Change	 	2016	 	2015	 	$ Change	 	% Change	
Direct	$	38.5	
 	 	$	31.5	
 	 	$	7.0	
 	 	22.2	%	 	$	74.1	
 	 	$	62.6	
 	 	$	11.5	
 	 	18.4	%	
OEM	32.1	
 	 	26.7	
 	 	5.4	
 	 	20.2	%	 	61.5	
 	 	54.3	
 	 	7.2	
 	 	13.3	%	
Total Infusion Therapy Revenue	$	70.6	
 	 	$	58.2	
 	 	$	12.4	
 	 	21.3	%	 	$	135.6	
 	 	$	116.9	
 	 	$	18.7	
 	 	16.0	%	

Direct infusion therapy sales increased for the three and six months ended June 30, 2016, as compared to the same period in the prior year, primarily due to sales of our SwabCap product-line, which was acquired through an acquisition in October 2015, and our Clave product-lines as a result of new customer sales and an increase in sales to existing customers. Partially offsetting these period increases was a decrease in sales of other infusion products.

OEM infusion therapy sales increased for the three and six months ended June 30, 2016, as compared to the same period in the prior year, primarily a result of the sales of our OEM SwabCap product and sales of our Clave product lines.

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Critical Care Revenue

The following table summarizes our total critical care revenue by direct and OEM distribution channels (in millions):

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Three months ended June 30,	 	Six months ended June 30,	
 	2016	 	2015	 	$ Change	 	% Change	 	2016	 	2015	 	$ Change	 	% Change	
Direct	$	13.2	
 	 	$	14.9	
 	 	$	(1.7	)	 	(11.4	)%	 	$	26.2	
 	 	$	28.5	
 	 	$	(2.3	)	 	(8.1	)%	
OEM	—	
 	 	0.2	
 	 	(0.2	)	 	(100.0	)%	 	—	
 	 	0.2	
 	 	(0.2	)	 	(100.0	)%	
Total Critical Care Revenue	$	13.2	
 	 	$	15.1	
 	 	$	(1.9	)	 	(12.6	)%	 	$	26.2	
 	 	$	28.7	
 	 	$	(2.5	)	 	(8.7	)%	

Direct critical care sales decreased for the three and six months ended June 30, 2016, as compared to the same period in the prior year, primarily due to a decline of both international and U.S. sales of both our hemodynamic monitoring and our closed blood sampling and conservation system products.

Oncology Revenue

The following table summarizes our total oncology revenue by direct and OEM distribution channels (in millions):

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Three months ended June 30,	 	Six months ended June 30,	
 	2016	 	2015	 	$ Change	 	% Change	 	2016	 	2015	 	$ Change	 	% Change	
Direct	$	8.9	
 	 	$	6.0	
 	 	$	2.9	
 	 	48.3	 %	 	$	17.3	
 	 	$	12.0	
 	 	$	5.3	
 	 	44.2	%	
OEM	3.8	
 	 	4.2	
 	 	(0.4	)	 	(9.5	)%	 	7.0	
 	 	6.9	
 	 	0.1	
 	 	1.4	%	
Total Oncology Revenue	$	12.7	
 	 	$	10.2	
 	 	$	2.5	
 	 	24.5	 %	 	$	24.3	
 	 	$	18.9	
 	 	$	5.4	
 	 	28.6	%	

Direct oncology sales increased for the three and six months ended June 30, 2016, as compared to the same period in the prior year, primarily due to increased direct sales in the U.S. These increases were a result of new customer sales and an increase in sales to existing customers of our ChemoLock and ChemoClave product.

OEM oncology sales marginally decreased during the three months ended June 30, 2016, as compared to the prior year comparable period due to a decrease in U.S. sales of our ChemoClave product, partially offset by an increase in international sales of the same product.

OEM oncology sales marginally increased during the six months ended June 30, 2016, as compared to the prior year comparable period due to an increase in international orders of the ChemoClave product mostly offset by a decrease in U.S. sales.
 
Gross margins

For the three and six months ended June 30, 2016 gross margins were 51.8% and 53.3%, respectively, as compared to 52.2% for the three and six months ended June 30, 2015. The 40 basis point decrease in gross margin for the three months ended June 30, 2016, as compared to the same period in the prior year was primarily due to certain manufacturing constraints, which caused higher cost for products manufactured in the first quarter that were sold in the second quarter. The 110 basis point increase in gross margin for the six months ended June 30, 2016, as compared to the same period in the prior year was primarily due to favorable foreign exchange rates on our operations expenses due to the decline in the Mexican Peso and favorable product mix partially offset by the impact of certain manufacturing constraints, mentioned above.

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Selling, general and administrative (“SG&A”) expenses

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Three months ended June 30,	 	Six months ended June 30,	
 	2016	 	2015	 	$ Change	 	% Change	 	2016	 	2015	 	$ Change	 	% Change	
SG&A	$	22.5	
 	 	$	20.3	
 	 	$	2.2	
 	 	10.8	%	 	$	44.5	
 	 	$	40.5	
 	 	$	4.0	
 	 	9.9	%	

SG&A expenses increased for the three months ended June 30, 2016, as compared to the same period in the prior year, primarily due to an increase of $1.5 million in compensation, $0.7 million in dealer fees and $0.3 million in commissions, partially offset by $0.5 million in lower medical device excise taxes and $0.4 million in lower legal expenses. The increase in compensation is in part due to filling positions that were open during 2015, additional employees retained as part of the acquired SwabCap product line, the general hiring and recruitment of new employees and increases in stock-based compensation issued to attract these employees. The increases in dealer fees and commissions were related to an increase in revenue on which they are calculated. The decrease in medical device excise tax expense was due to the elimination of the tax in the current period due to Congress temporarily suspending this tax for the 2016-2017 two-year period. The decrease in legal expenses was due to less litigation.

SG&A expenses increased for the six months ended June 30, 2016, as compared to the same period in the prior year primarily due to an increase of $3.3 million in compensation, $0.7 million in higher dealer fees, and $0.5 million in commissions partially offset by $0.9 million in lower legal expenses and $0.9 million in lower medical device excise taxes. The reasons for the changes are the same as indicated above with respect to the three months ended June 30, 2016.

Research and development (“R&D”)

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
 	Three months ended June 30,	 	Six months ended June 30,	
 	2016	 	2015	 	$ Change	 	% Change	 	2016	 	2015	 	$ Change	 	% Change	
R&D	$	3.3	
 	 	$	3.1	
 	 	$	0.2	
 	 	6.5	%	 	$	6.7	
 	 	$	7.4	
 	 	$	(0.7	)	 	(9.5	)%	

R&D expenses increased for the three months ended June 30, 2016, as compared to the same period in the prior year primarily due to higher R&D project expenses partially offset by a decrease in project costs related to our Cogent TM  2-in-1 hemodynamic monitoring system, which received FDA 510(k) clearance during the second quarter of 2016.

R&D expenses decreased for the six months ended June 30, 2016, as compared to the same period in the prior year primarily due to lower stock based compensation and lower R&D project expenses year-to-date related to our Cogent 2-in-1 hemodynamic monitoring system.

Legal settlement charges

Legal settlement charges were $7.1 million, or 4.0% of revenue for the six months ended June 30, 2015. On April 2, 2015, an arbitrator ruled on a breach of contract claim between us and Hospira, awarding Hospira $8.2 million Canadian dollars ($6.5 million U.S. dollars). The arbitrator also ruled that we pay 75% of Hospira's legal fees and expenses, which were $0.7 million dollars. We have fully paid the above mentioned legal fees and expenses.

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Restructuring and strategic transaction

Restructuring and strategic transaction expenses were $1.5 million for each of the three and six months ended June 30, 2016. Restructuring charges of $0.2 million were related to residual expenses for the closure of our Slovakian manufacturing facility and we incurred $0.2 million related to other restructuring activities. We incurred $1.1 million in transaction costs related to our 2015 acquisition of EXC Holding Corp. ("EXC") and to our second quarter 2016 acquisition of Tangent.

Bargain purchase gain

As a result of the Tangent acquisition, we immediately recognized a $1.1 million bargain purchase gain that represented the excess of the estimated fair market value of the identifiable tangible and intangible assets acquired and liabilities assumed, net of deferred tax attributes over the total purchase consideration. The bargain purchase was driven by our ability to realize acquired deferred tax assets.

Other income

Other income was $0.1 million and $0.2 million for the three and six months ended June 30, 2016, as compared to $0.2 million and $0.8 million for the three and six months ended June 30, 2015.

Income taxes

Income taxes were accrued at an estimated effective tax rate of 31% and 28% for the three and six months ended June 30, 2016, respectively, as compared to 34% and 27% for the three and six months ended June 30, 2015, respectively. 

The effective tax rate for the three and six months ended June 30, 2016 differs from the federal statutory rate principally because of the effect of foreign and state income taxes, tax credits, deductions for domestic production activities, and included material discrete tax benefits related to the adoption of ASU 2016-09, see below.

The effective tax rate during the three and six months ended June 30, 2016 included a material discrete tax benefit of $0.8 million and $3.1 million, respectively, related to the adoption of Accounting Standard Update ("ASU") 2016-09, Compensation - Stock Compensation (Topic 718): Improvements to Employee Share-Based Payment Accounting during the second quarter of 2016. The income tax benefit was treated as a discrete item when determining the annual estimated effective tax rate. See Note 2, New Accounting Pronouncements for further detail.
The effective tax rates for the three and six months ended 2015 differs from the federal statutory rate principally because of the effect of foreign and state income taxes, tax credits, deductions for domestic production activities and material discrete tax benefits related to the impact of changes in estimates of tax reserves related to uncertainties in income taxes as a result of the favorable conclusion of recent federal and state examinations.

Liquidity and Capital Resources
 
During the first six months of 2016, our cash, cash equivalents and investment securities increased by $23.2 million from $377.4 million at December 31, 2015 to $400.6 million at June 30, 2016.
 
Cash Flows from Operating Activities

Our cash provided by operations for the six months ended June 30, 2016 was $41.8 million. Net income plus adjustments for non-cash net expenses contributed $51.0 million to cash provided by operations, and cash used by changes in operating assets and liabilities was $9.2 million. The changes in operating assets and liabilities included a $6.0 million decrease in accrued liabilities, a $5.5 million increase in inventories, a $3.8 million increase in prepaid expenses and other assets, and a $2.5 million increase in accounts receivable, partially offset by $4.8 million in net changes to income taxes and deferred income taxes and a $3.8 million increase in accounts payable. The decrease in accrued liabilities was primarily due to the pay-out of fiscal year 2015 accrued bonuses in February of 2016, the payment of accrued restructuring charges related to the closure of our Slovakian manufacturing facility and the payment of acquisition-related accruals from our 2015 EXC acquisition. The increase in inventories was primarily due to building finished good safety stock, to support better customer deliveries, raw materials related to our Slovakia plant closure, and related transfer to our Mexico plant, and inventory associated with the acquired SwabCap product-line. The increase in prepaid expenses and other assets was primarily due to amounts owed by employees for the exercise of their stock options partially offset by a decrease in prepaid insurance due to amortization. The increase in accounts receivable was due to an increase in revenue. The net changes in income taxes was a result of the timing

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of payments for cash tax purposes, which includes true-ups for 2015 overpayment and 2016 estimated taxes. The increase in accounts payable was a result of timing.

Our cash provided by operations for the six months ended June 30, 2015 was $29.2 million, which includes a retrospective adjustment to include $3.4 million in excess tax benefits as an operating item due to the implementation of ASU 2016-09, Compensation - Stock Compensation (Topic 718): Improvements to Employee Share-Based Payment Accounting during the second quarter of 2016, see Note 2 for more details. Net income plus adjustments for non-cash net expenses contributed $39.5 million to cash provided by operations, which was partially offset by a $10.3 million decrease in cash provided by operating assets and liabilities, retrospectively, adjusted for the impact of the aforementioned ASU. The $5.5 million increase in accounts receivable was the largest change in operating assets and liabilities. The increase in accounts receivable is primarily due to higher revenue in the second quarter of 2015 compared to the fourth quarter of 2014.

Cash Flows from Investing Activities

The following table summarizes the changes in our investing cash flows (in thousands):

 	Six Months Ended June 30,	 	 	 	
 	2016	 	2015	 	Change	 	
Investing Cash Flows:	 	 	 	 	 	 	
Purchases of property and equipment	$	(9,112	)	 	$	(5,005	)	 	$	(4,107	)	(1) 	
Proceeds from sale of assets	1	
 	 	34	
 	 	(33	)	 	
Business acquisitions, net of cash acquired	(2,606	)	 	—	
 	 	(2,606	)	(2) 	
Intangible asset additions	(513	)	 	(440	)	 	(73	)	 	
Purchases of investment securities	(18,106	)	 	(17,092	)	 	(1,014	)	 	
Proceeds from sale of investment securities	31,765	
 	 	49,555	
 	 	(17,790	)	(3) 	
Net cash provided by investing activities	$	1,429	
 	 	$	27,052	
 	 	$	(25,623	)	 	
______________________________
(1)    Our purchases of property and equipment will vary from period to period based on additional investments needed to support new and existing products and expansion of our manufacturing facilities.
 	 	
(2) 	Our business acquisitions will vary from period to period based upon our current growth strategy and our ability to execute on desirable target companies. During the second quarter of 2016 we acquired Tangent for $2.6 million in cash.	
(3)    Net proceeds from the sale of our investment securities decreased during the six months of 2016, as compared to the comparable prior year period, due to certain corporate bonds that had larger investment balances and maturity dates within the first six months ended June 30, 2015.

While we can provide no assurances, we estimate that our capital expenditures in 2016 will approximate $18.0 million to $20.0 million. We anticipate making additional investments in molds, machinery and equipment in our manufacturing operations in the U.S. and Mexico to support new and existing products and in IT to benefit world-wide operations. Additionally, we are in the process of expanding our Mexico manufacturing plant for the anticipated increase in operations as a result of our Slovakian plant closure. We expect to use our cash and investments to fund our capital purchases. These planned amounts of spending are estimates and actual spending may substantially differ from these amounts.

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Cash Flows from Financing Activities
 
The following table summarizes the changes in our financing cash flows (in thousands):    

 	Six Months Ended June 30,	 	 	 	
 	2016	 	2015	 	Change	 	
Financing Cash Flows:	 	 	 	 	 	 	
Proceeds from exercise of stock options	$	7,796	
 	 	$	5,797	
 	 	$	1,999	
 	(1) 	
Proceeds from employee stock purchase plan	1,197	
 	 	1,041	
 	 	156	
 	 	
Purchase of treasury stock	(16,911	)	 	(1,435	)	 	(15,476	)	(2) 	
Net cash (used in) provided by financing activities	$	(7,918	)	 	$	5,403	
 	 	$	(13,321	)	 	
______________________________
(1)   Proceeds from the exercise of stock options will vary from period to period based on the volume of options exercised and the exercise price of the specific options exercised.
(2) During the six months ended June 30, 2016, we purchased 174,885 shares of our common stock under our share purchase plan on the open market for $15.3 million. Additionally, our employees surrendered 17,661 shares of our common stock from vested restricted stock awards as consideration for approximately $1.6 million in minimum statutory withholding obligations paid on their behalf.

In July 2010, our Board of Directors approved a share purchase plan to purchase up to $40.0 million of our common stock.  As of June 30, 2016, we had purchased $32.8 million of our common stock pursuant to this plan, leaving a balance of $7.2 million available for future purchases. This plan has no expiration date. We may purchase additional shares in future quarters and expect we would use our cash and investments to fund the share purchases. 

We have a substantial cash and investment security position generated from profitable operations and stock sales, principally from the exercise of employee stock options.  We maintain this position to fund our growth, meet increasing working capital requirements, fund capital expenditures, buy back our common stock on an opportunistic basis and to take advantage of acquisition opportunities that may arise.  Our primary investment goal is capital preservation.

As of June 30, 2016, we had $20.6 million of cash and cash equivalents held in local currency by our foreign subsidiaries. If these funds were needed for our operations in the U.S., we would be required to accrue and pay U.S. taxes for a portion of any repatriated funds. However, we expect to permanently reinvest these funds outside of the U.S. and, based on our current plans, we do not presently anticipate a need to repatriate them to fund our U.S. operations.
 
We believe that our existing cash, cash equivalents and investment securities along with funds expected to be generated from future operations will provide us with sufficient funds to finance our current operations for the next twelve months.  In the event that we experience illiquidity in our investment securities, downturns or cyclical fluctuations in our business that are more severe or longer than anticipated or if we fail to achieve anticipated revenue and expense levels, we may need to obtain or seek alternative sources of capital or financing, and we can provide no assurances that the terms of such capital or financing will be available to us on favorable terms, if at all.

Off Balance Sheet Arrangements
 
In the normal course of business, we have agreed to indemnify our officers and directors to the maximum extent permitted under Delaware law and to indemnify customers as to certain intellectual property matters related to sales of our products.  There is no maximum limit on the indemnification that may be required under these agreements.  Although we can provide no assurances, we have never incurred, nor do we expect to incur, any material liability for indemnification.

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Contractual Obligations
 
As of June 30, 2016, there were no material changes to our contractual obligations from the amounts reported in our 2015 Form 10-K, except with respect to our purchase obligations as follows (in thousands):

 	 	 	 	 	
Contractual Obligations	 	2016	
Purchase obligations	 	$	5,104	
 	
 	 	$	5,104	

Critical Accounting Policies
 
In our Annual Report on Form 10-K for the year ended December 31, 2015, we identified the critical accounting policies which affect our more significant estimates and assumptions used in preparing our consolidated financial statements. We have not changed these policies from those previously disclosed in our Annual Report.
 
New Accounting Pronouncements
 
See Note 2 to Part I, Item 1.  Financial Statements.

Forward Looking Statements
 
Various portions of this Quarterly Report on Form 10-Q, including this Management’s Discussion and Analysis of Financial Condition and Results of Operations, and documents referenced herein, describe trends in our business and finances that we perceive and state some of our expectations and beliefs about our future. These statements about the future are “forward looking statements,” within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, and we identify them by using words such as "anticipate," "believe," "expect," "estimate," "intend," "plan," "will," "continue," "could," "may," and by similar expressions and statements about aims, goals and plans. The forward looking statements are based on the best information currently available to us and assumptions that we believe are reasonable, but we do not intend the statements to be representations as to future results. They include, without limitation, statements about:
 	 	
•	future growth; future operating results and various elements of operating results, including future expenditures and effects with respect to sales and marketing and product development and acquisition efforts; future sales and unit volumes of products; expected increases and decreases in sales; deferred revenue; accruals for restructuring charges, future license, royalty and revenue share income; production costs; gross margins; litigation expense; future SG&A and R&D expenses; manufacturing expenses; future costs of expanding our business; income; losses; cash flow; amortization; source of funds for capital purchases and operations; future tax rates; alternative sources of capital or financing; changes in working capital items such as receivables and inventory; selling prices; and income taxes;	

•	factors affecting operating results, such as shipments to specific customers; reduced dependence on current proprietary products; loss of a strategic relationship; change in demand; domestic and international sales; expansion in international markets, selling prices; future increases or decreases in sales of certain products and in certain markets and distribution channels; maintaining strategic relationships and securing long-term and multi-product contracts with large healthcare providers and major buying organizations; increases in systems capabilities; introduction, development and sales of new products, acquisition and integration of businesses and product lines, including SwabCap (EXC) and Tangent; benefits of our products over competing systems; qualification of our new products for the expedited Section 510(k) clearance procedure; possibility of lengthier clearance process for new products; planned increases in marketing; warranty claims; rebates; product returns; bad debt expense; amortization expense; inventory requirements; lives of property and equipment; manufacturing efficiencies and cost savings; unit manufacturing costs; establishment or expansion of production facilities inside or outside of the U. S.; planned new orders for machinery and equipment; adequacy of production capacity; results of R&D; our plans to repurchase shares of our common stock; asset impairment losses; relocation of manufacturing facilities and personnel and plans to sell our Slovakia manufacturing facility; effect of expansion of manufacturing facilities on production efficiencies and resolution of production inefficiencies; the effect of costs to customers and delivery times; business	

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seasonality and fluctuations in quarterly results; customer ordering patterns and the effects of new accounting pronouncements; and
 	 	
•	new or extended contracts with manufacturers and buying organizations; dependence on a small number of customers; loss of larger distributors and the ability to locate other distributors; the impact of the Pfizer acquisition of Hospira; future sales to and revenue from Pfizer and the importance of Pfizer to our growth; effect of the current relationship with Pfizer and the settlement with Hospira, including its effect on future revenue and our positioning with respect to new product introductions and market share; growth of our products in future years; design features of Clave products; the outcome of our strategic initiatives; regulatory approvals and compliance; outcome and impact of litigation; patent protection and intellectual property landscape; patent infringement claims and the impact of newly issued patents on other medical devices; competitive and market factors, including continuing development of competing products by other manufacturers; improved production processes and higher volume production; innovation requirements; consolidation of the healthcare provider market and downward pressure on selling prices; distribution or financial capabilities of competitors; healthcare reform legislation; use of treasury stock; working capital requirements; liquidity and realizable value of our investment securities; future investment alternatives; foreign currency denominated financial instruments; foreign exchange risk; commodity price risk; our expectations regarding liquidity and capital resources over the next twelve months; plans to convert existing space; capital expenditures; our planned reinvestment of cash and cash equivalents held by our foreign subsidiaries; acquisitions of other businesses or product lines, indemnification liabilities and contractual liabilities.	

 Forward-looking statements involve certain risks and uncertainties, which may cause actual results to differ materially from those discussed in each such statement.  First, one should consider the factors and risks described in the statements themselves or otherwise discussed herein. Those factors are uncertain, and if one or more of them turn out differently than we currently expect, our operating results may differ materially from our current expectations.
 
Second, investors should read the forward looking statements in conjunction with the Risk Factors discussed in Part I, Item 1A of our Annual Report on Form 10-K with the SEC for the year ended December 31, 2015 and our other reports and registration statements filed with the SEC.  Also, actual future operating results are subject to other important factors and risks that we cannot predict or control, including without limitation, the following:
 	 	
•	general economic and business conditions, both in the U.S. and internationally;	

•	unexpected changes in our arrangements with Pfizer or our other large customers;	

•outcome of litigation;

•fluctuations in foreign exchange rates and other risks of doing business internationally;

•increases in labor costs or competition for skilled workers;

•increases in costs or availability of the raw materials need to manufacture our products;

•the effect of price and safety considerations on the healthcare industry;

•competitive factors, such as product innovation, new technologies, marketing and distribution strength and price erosion;

•the successful development and marketing of new products;

•unanticipated market shifts and trends;

•the impact of legislation affecting government reimbursement of healthcare costs;
 	 	
•	changes by our major customers and independent distributors in their strategies that might affect their efforts to market our products;	

•the effects of additional governmental regulations;

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•unanticipated production problems; and

•the availability of patent protection and the cost of enforcing and of defending patent claims.

The forward-looking statements in this report are subject to additional risks and uncertainties, including those detailed from time to time in our other filings with the Securities and Exchange Commission. These forward-looking statements are made only as of the date hereof and, except as required by law, we undertake no obligation to update or revise any of them, whether as a result of new information, future events or otherwise.

Item 3.	Quantitative and Qualitative Disclosures about Market Risk	
 
Financial Market Risk

We had a portfolio of government bonds, corporate bonds, U.S. Treasury securities, commercial paper and certificates of deposit of $27.7 million as of June 30, 2016.  The securities are all “investment grade”, comprised of $8.1 million of pre-refunded municipal securities, $15.4 million of corporate bonds, $3.0 million of U.S. Treasury securities, $0.7 million of commercial paper and $0.5 million of certificates of deposit.  The pre-refunded municipal securities are fully escrowed by U.S. government Treasury bills with low market risk.
 
Our future earnings are subject to potential increase or decrease because of changes in short-term interest rates. Generally, each one-percentage point change in the discount rate will cause our overall yield to change by two-thirds to three-quarters of a percentage point, depending upon the relative mix of our portfolio and market conditions specific to the securities in which we invest.  Two-thirds to three-quarters of a percentage point change in our earnings on investment securities would create a change of approximately $0.3 million to investment income based on the investment securities balance at June 30, 2016.
 
Foreign Exchange Risk    

We have foreign currency exchange risk related to foreign-denominated cash, short-term investments, accounts
receivable and accounts payable. In our European operations, our net Euro asset position at June 30, 2016 was
approximately €17.8 million. We also have approximately €79.6 million in Euro denominated cash and investment accounts
held by our corporate entity. A 10% change in the conversion of the Euro to the U.S. dollar for our cash and investments,
accounts receivable, accounts payable and accrued liabilities from the June 30, 2016 spot rate would impact our
consolidated amounts on these balance sheet items by approximately $10.8 million, or 2.7% of these consolidated net assets. We expect that in the future, with the growth of our European distribution operations, net Euro denominated instruments will continue to increase. We currently do not hedge our foreign currency exposures.

Sales from the U.S. to foreign distributors are denominated in U.S. dollars, Euros, South African Rand and Australian dollars. We have manufacturing, sales and distribution facilities in several countries and we conduct business transactions denominated in various foreign currencies, although principally the Euro and Mexican Peso. A 10% change in the conversion of the Mexican Peso to the U.S. dollar from the average exchange rate we experienced in 2016 and our manufacturing spending from 2016 would have impacted 2016 cost of goods sold by approximately $0.6 million. To date, the change in the conversion of the Euro to the U.S. dollar has not had a material impact to our operating earnings.

Item 4.	Controls and Procedures	
 
Disclosure Controls and Procedures
 
Our principal executive officer and principal financial officer have concluded, based on their evaluation of our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Securities Exchange Act of 1934), as of the end of the period covered by this Report, that our disclosure controls and procedures are effective to ensure that the information we are required to disclose in the reports that we file or submit under the Exchange Act is accumulated and communicated to our management, including our principal executive officer and principal financial officer, as appropriate, to allow timely decisions regarding required disclosure and that such information is recorded, processed, summarized and reported within the time periods specified in the rules and forms of the SEC.
 
There was no change in our internal control over financial reporting during the quarter ended June 30, 2016 that has materially affected or is reasonably likely to materially affect our internal control over financial reporting.

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PART II - OTHER INFORMATION

Item 1.	Legal Proceedings	
 
We are from time to time involved in various other legal proceedings, either as a defendant or plaintiff, most of which are routine litigation in the normal course of business. We believe that the resolution of the legal proceedings in which we are involved will not have a material adverse effect on our financial position or results of operations.

Item 1A.	Risk Factors	
 
In evaluating an investment in our common stock, investors should consider carefully, among other things, the risk factors previously disclosed in Part I, Item 1A of our Annual Report on Form 10-K filed with the SEC for the year ended December 31, 2015, as well as the information contained in this Quarterly Report and our other reports and registration statements filed with the SEC.  There have been no material changes in the risk factors as previously disclosed under “Risk Factors” in Part I, Item 1A of our Annual Report on Form 10-K with the SEC for the year ended December 31, 2015.

Item 2.	Unregistered Sales of Equity Securities and Use of Proceeds	
 
In July 2010, our Board of Directors approved a common stock purchase plan to purchase $40.0 million of our common stock.  This plan has no expiration date. We are not obligated to make any purchases under our stock purchase program. Subject to applicable state and federal corporate and securities laws, purchases under a stock purchase program may be made at such times and in such amounts as we deem appropriate. Purchases made under our stock purchase program can be discontinued at any time we feel additional purchases are not warranted.

The following is a summary of our stock repurchasing activity during the second quarter of 2016:

 	 	 	 	 	 	 	 	 	 	 	 	 	 	 	
Period	 	Shares
purchased(1)	 	Average
price paid
per share	 	Shares
purchased as
part of a
publicly
announced
program	 	Approximate
dollar value that
may yet be
purchased under
the program	
04/01/2016 — 04/30/2016	 	—	
 	 	$	—	
 	 	—	
 	 	$	7,169,000	
 	
05/01/2016 — 05/31/2016	 	—	
 	 	$	—	
 	 	—	
 	 	$	7,169,000	
 	
06/01/2016 — 06/30/2016	 	133	
 	 	$	106.94	
 	 	—	
 	 	$	7,169,000	
 	
Second quarter of 2016 total	 	133	
 	 	$	106.94	
 	 	—	
 	 	$	7,169,000	
 	
____________________________
 	 	
(1) 	Represents shares of our common stock that were surrendered to us in June 2016 by employees to satisfy minimum statutory income tax withholding obligations in connection with the vesting of their restricted stock units.	

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Item 6. Exhibits

 	 	 	
Exhibit 31.1	 	Certification of Chief Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002	
 	 	 	
Exhibit 31.2	 	Certification of Chief Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002	
 	 	 	
Exhibit 32.1	 	Certifications of Chief Executive Officer and Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002	
 	 	 	
Exhibit 101.INS	 	XBRL Instance Document	
 	 	 	
Exhibit 101.SCH	 	XBRL Taxonomy Extension Schema Document	
 	 	 	
Exhibit 101.CAL	 	XBRL Taxonomy Extension Calculation Linkbase Document	
 	 	 	
Exhibit 101.DEF	 	XBRL Taxonomy Extension Definition Linkbase Document	
 	 	 	
Exhibit 101.LAB	 	XBRL Taxonomy Extension Label Linkbase Document	
 	 	 	
Exhibit 101.PRE	 	XBRL Taxonomy Extension Presentation Linkbase Document	

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Signature
 
Pursuant to the requirements of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.
 
ICU Medical, Inc.

 	 	 	
(Registrant)	 	 	
 	 	 	
/s/ Scott E. Lamb	Date:	August 9, 2016	
Scott E. Lamb	 	 	
Chief Financial Officer	 	 	
(Principal Financial Officer)	 	 	

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Exhibit Index

 	 	 	
 	 	 	
Exhibit 31.1	 	Certification of Chief Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002	
 	 	 	
Exhibit 31.2	 	Certification of Chief Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002	
 	 	 	
Exhibit 32.1	 	Certifications of Chief Executive Officer and Chief Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002	
 	 	 	
Exhibit 101.INS	 	XBRL Instance Document	
 	 	 	
Exhibit 101.SCH	 	XBRL Taxonomy Extension Schema Document	
 	 	 	
Exhibit 101.CAL	 	XBRL Taxonomy Extension Calculation Linkbase Document	
 	 	 	
Exhibit 101.DEF	 	XBRL Taxonomy Extension Definition Linkbase Document	
 	 	 	
Exhibit 101.LAB	 	XBRL Taxonomy Extension Label Linkbase Document	
 	 	 	
Exhibit 101.PRE	 	XBRL Taxonomy Extension Presentation Linkbase Document	

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Exhibit 31.1
 
CERTIFICATION OF CHIEF EXECUTIVE OFFICER PURSUANT TO SECTION 302 OF THE SARBANES-OXLEY ACT OF 2002
 
I, Vivek Jain, certify that:
 	 	
1.	I have reviewed this quarterly report on Form 10-Q of ICU Medical, Inc.;	

2.	Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;	

3.	Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;	

4.	The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:	

a)	Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;	

b)	Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;	

c)	Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and	

d)	Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and	

5.	The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):	

a)	All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and	

b)	Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.	

 	
 	 	 	
Date:	August 9, 2016	/s/ Vivek Jain	
 	 	Chief Executive Officer	

 	

Exhibit 31.2
 
CERTIFICATION OF CHIEF FINANCIAL OFFICER PURSUANT TO SECTION 302 OF THE SARBANES-OXLEY ACT OF 2002
 
I, Scott E. Lamb, certify that:

1.	 I have reviewed this quarterly report on Form 10-Q of ICU Medical, Inc.;	

2.	Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report;	

3.	Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;	

4.	The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in Exchange Act Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have:	

a)	Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared;	

b)	Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles;	

c)	Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and	

d)	Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and	

5.	The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):	

a)	All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and	

b)	Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting.	

 	 	 	
Date:	August 9, 2016	/s/ Scott E. Lamb	
 	 	Chief Financial Officer	

 	

Exhibit 32.1
 
CERTIFICATION OF CHIEF EXECUTIVE OFFICER
PURSUANT TO
18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
 
In connection with the Quarterly Report of ICU Medical, Inc. (the “Company”) on Form 10-Q for the period ended June 30, 2016 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I, Vivek Jain, Chief Executive Officer of the Company, certify, pursuant to 18 U.S.C. § 1350, as adopted pursuant to § 906 of the Sarbanes-Oxley Act of 2002, that:

(1)	The Report fully complies with the requirements of section 13(a) or 15(d) of the Securities Exchange Act of 1934; and	

(2)	The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.	

 	
 	 	
August 9, 2016	/s/ Vivek Jain	
 	Vivek Jain	
 
CERTIFICATION OF CHIEF FINANCIAL OFFICER
PURSUANT TO
18 U.S.C. SECTION 1350,
AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
 
In connection with the Quarterly Report of ICU Medical, Inc. (the “Company”) on Form 10-Q for the period ended June 30, 2016 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), I, Scott E. Lamb, Chief Financial Officer of the Company, certify, pursuant to 18 U.S.C. § 1350, as adopted pursuant to § 906 of the Sarbanes-Oxley Act of 2002, that:

(1)	The Report fully complies with the requirements of section 13(a) or 15(d) of the Securities Exchange Act of 1934; and	

(2)	The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.	

 	 	
August 9, 2016	/s/ Scott E. Lamb	
 	Scott E. Lamb