FDAFDA · Food and drugs·Recall number Z-0495-2019
Vanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126
Published November 28, 2018 · Recall initiated: October 22, 2018
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Label on the outer carton or the patient labels does not match label on the inner sterile packaging
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Zimmer Biomet, Inc.
- Distributor
- AR, MO, MN, NJ, NY, OH, MN , NJ, VA
- Lot
- Lot Number: J6255863 UDI: (01)00880304270794(17)280411(10)J6265594
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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