FDAFDA · Food and drugs·Recall number Z-2405-2024
REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly
Published July 24, 2024 · Recall initiated: May 31, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Stryker Sustainability Solutions
- Distributor
- US Nationwide distribution in the states of CA, CO, IL, MI, OR, WI.
- Lot
- Lot: 0000564862/ UDI: 00885825015411
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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