Bronstein, Gewirtz & Grossman, LLC is investigating potential claims on behalf of purchasers of ICU Medical, Inc. (“ICU Medical” or “the Company”) (NASDAQ: ICUI). Investors who purchased ICU Medical securities are encouraged to obtain additional information and assist the investigation.

The investigation concerns whether ICU Medical has violated federal securities laws.

Investigation Details

On April 22, 2025, ICU Medical received a warning letter from the Food and Drug Administration (“FDA”). According to the FDA, the Company “made multiple changes to the Medfusion Model 4000 Syringe Infusion Pump and CADD Solis VIP Ambulatory Infusion Pump that could significantly affect the safety or effectiveness of these devices.” The FDA states that the Company’s pumps were “adulterated” and “misbranded,” with modifications that “can significantly impact the functionality of the device with respect to the infusion pumps delivery profile, alarm functionality, etc., and affect the device’s risk profile.” Following this news, ICU Medical stock dropped.

What’s Next?

If you are aware of any facts relating to this investigation or purchased ICU Medical securities, you can assist this investigation. You can also contact Peretz Bronstein or his client relations manager, Nathan Miller, of Bronstein, Gewirtz & Grossman, LLC: 332-239-2660