Reported Nov 28, 2018 · Terminated
Vanguard Knee System -PS Open Box Femoral Right, 65 mm Item Number:183108
Zimmer Biomet, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Zimmer Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
- Vanguard Knee System -PS Open Box Femoral Right, 65
- mm Item Number183108
- Lot codes and dates
- Lot NumberJ6265594
- UDI(01)00880304270893(17)280411(10)J6255863
- Amount recalled
- 8 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Label on the outer carton or the patient labels does not match label on the inner sterile packaging
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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