ICU MEDICAL INC quarterly report, Q2 FY2013

ICU Medical, Inc. — Q2 2013 Form 10-Q

Reporting period: Three and six months ended June 30, 2013; comparisons are with the corresponding 2012 periods. Financial statements are unaudited. ICU Medical develops, manufactures and sells medical devices for infusion therapy, critical care and oncology.

Financial highlights

MetricQ2 2013Q2 2012First half 2013First half 2012
Total revenue$78.7 million$77.3 million$153.0 million$152.8 million
Gross profit / margin$38.0 million / 48%$39.1 million / 51%$74.8 million / 49%$74.0 million / 48%
Operating income$11.0 million$13.5 million$23.0 million$24.9 million
Net income$7.4 million$9.1 million$16.1 million$16.8 million
Diluted EPS$0.48$0.63$1.06$1.16
Operating cash flowNot separately reported for quarterNot separately reported for quarter$26.0 million$31.5 million
  • Q2 revenue rose about 2%, while net income declined about 19%. First-half revenue was essentially flat and net income declined about 4%.
  • Q2 gross margin fell three percentage points, which management attributed primarily to manufacturing inefficiencies and unfavorable Mexican peso exchange-rate effects, partly offset by favorable product mix. First-half margin improved one point, primarily from product mix.
  • At June 30, cash and cash equivalents were $170.6 million and investment securities were $73.4 million, for combined cash and investments of $244.0 million, up from $226.2 million at year-end 2012. Total assets were $451.6 million; current liabilities were $28.0 million. The balance sheet reports no debt.
  • First-half investing cash use was $8.1 million, including $11.8 million in property and equipment purchases. Financing activities provided $6.5 million. The filing reports no borrowing facility or debt balance.

Business trends and material changes

  • Product mix was uneven: first-half oncology revenue increased 30% to $17.5 million; critical care fell 14% to $25.4 million amid competition; infusion therapy increased 1% to $103.6 million. In Q2, oncology rose 32%, critical care declined 19%, and infusion therapy rose 3% year over year.
  • Hospira accounted for 40% of first-half revenue in both 2013 and 2012, and 39% of accounts receivable at June 30, 2013. Q2 Hospira revenue was 42% of total, versus 38% a year earlier. Hospira’s planned first-quarter inventory reduction contributed to lower first-half Clave shipments.
  • First-half domestic sales declined 3%, while international sales increased 8%. Critical care competition weighed on both domestic and international sales.
  • SG&A increased to $46.0 million from $43.7 million for the first half; the 2013 medical device excise tax contributed $0.9 million to the increase. R&D rose to $5.8 million from $5.4 million.

Outlook, risks and contingencies

  • Management estimated 2013 capital expenditures of $23–$28 million, including planned Salt Lake City manufacturing-space and clean-room improvements, equipment and mold purchases, and IT investment. It expected to fund spending from cash and investments.
  • Management expected modest 2013 growth in infusion therapy and oncology, lower critical care sales due to competition, SG&A of approximately 28% of revenue, R&D of approximately 3% of revenue, and an effective tax rate near 33%. These are estimates and not guarantees.
  • The company said existing cash, investments and expected operating cash generation should fund operations for the next 12 months. It held $15.0 million of cash at foreign subsidiaries. Management noted that prolonged business weakness or investment-security illiquidity could require alternative financing.
  • Customer concentration, especially dependence on Hospira and its distribution arrangements, is a significant risk. Other stated risks include competitive pressure, new-product execution, manufacturing problems, foreign exchange exposure, raw-material costs and healthcare regulation. A 10% euro exchange-rate change was estimated to affect relevant net balance-sheet assets by about $6.9 million; the company did not hedge foreign-currency exposure.
  • ICU Medical continued patent litigation against RyMed Technologies. A jury had found infringement and patent validity in 2010; a court ruling on RyMed’s prosecution-history-estoppel defense remained pending, after which damages, if any, would be determined. Management did not expect other routine legal matters to materially harm results.
  • No material changes to the risk factors from the 2012 Form 10-K were reported. Management stated disclosure controls were effective and there was no material change in internal control over financial reporting during the quarter.

Important facts for investors to verify

  • Hospira’s share of revenue and receivables, the terms and duration of its distribution agreements, and the effect of customer inventory changes.
  • Whether gross-margin pressure from manufacturing inefficiencies and currency effects persists, and whether critical care competition continues to reduce sales.
  • Actual capital expenditures versus the $23–$28 million estimate and the expected capacity benefits of facility investments.
  • Progress and potential financial outcomes of the RyMed litigation, including any damages or appeals.
  • Investment portfolio liquidity and interest-rate exposure, along with the effect of unhedged euro and Mexican peso movements.