ICU Medical Inc.: Device Recall

Recall #Z-1101-2026 · 12/19/2025

Class II: Risk

Recall Details

Recall Number
Z-1101-2026
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

Portex Spinal Tray, Item No. A3729-24 A3595

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.

View all recalls by ICU Medical Inc. →

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.