Reported Mar 6, 2019 · Terminated
Vanguard Knee System Series-A Standard Patella sizes 34mm Item Number: 184766
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 Series-A
- Standard Patella sizes 34mm Item Number184766
- Lot codes and dates
- Lot Number381800
- UDI Number(01)00880304434349(17)230301(10)381800
- Lot NUmber400030 (01)00880304434349(17)230329(10)400030
- Amount recalled
- 90 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
Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
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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