REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Reported: July 24, 2024 Initiated: May 31, 2024 #Z-2405-2024
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.
Details
- Recalling Firm
- Stryker Sustainability Solutions
- Units Affected
- 90 units
- Distribution
- US Nationwide distribution in the states of CA, CO, IL, MI, OR, WI.
- Location
- Tempe, AZ
Frequently Asked Questions
What product was recalled? ▼
REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly. Recalled by Stryker Sustainability Solutions. Units affected: 90 units.
Why was this product recalled? ▼
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 24, 2024. Severity: Moderate. Recall number: Z-2405-2024.
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