Recall Z-2405-2024— Stryker Sustainability Solutions
Class II · Ongoing
Class II FDA medical device recall by Stryker Sustainability Solutions, initiated 2024-05-31. FDA's recall record names no specific 510(k) clearance for this event. Product: REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly. Reason: Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder..
- Recalling firm
- Stryker Sustainability Solutions
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-05-31
- Firm location
- Tempe, AZ, United States
Product description
REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Reason for recall
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
Data sourced from openFDA. This site is unofficial and independent of the FDA.