ICU Medical Inc.: Device Recall
Recall #Z-1100-2026 · 12/19/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1100-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- ICU Medical Inc.
- Status
- Ongoing
- Date Initiated
- 12/19/2025
- Location
- Minneapolis, MN, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 64290 total
Reason for Recall
Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to blood leakage during sampling of arterial blood or leakage during fluid delivery.
Product Description
Pulsator Arterial Blood Sampling Kit, Item Numbers 4044EG-1 4080P-2 4084P-1 4080PE 4080PG
Distribution Pattern
US Nationwide distribution in the states of CA, FL, IL, IN, MA, MI, MN, MO, NE, NJ, NY, OH, OK, TX, WA.
Other Recalls by ICU Medical Inc.
- Class II: Risk 12/19/2025
- Class II: Risk 12/19/2025
- Class II: Risk 12/15/2025
- Class II: Risk 12/15/2025
- Class II: Risk 12/15/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.