Stryker Sustainability Solutions: Device Recall
Recall #Z-2405-2024 · 05/31/2024
Class II: Risk
Recall Details
- Recall Number
- Z-2405-2024
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Stryker Sustainability Solutions
- Status
- Ongoing
- Date Initiated
- 05/31/2024
- Location
- Tempe, AZ, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 90 units
Reason for Recall
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
Product Description
REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Distribution Pattern
US Nationwide distribution in the states of CA, CO, IL, MI, OR, WI.
Other Recalls by Stryker Sustainability Solutions
- Class II: Risk 09/24/2025
- Class II: Risk 07/02/2024
- Class II: Risk 05/10/2024
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.