Reported Jun 3, 2020 · Terminated
Knee Products: 184762 Knees Vanguard Knee System, Series-A Standard Patella, 28 MM; 184764 Knees Vanguard Knee System,…
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: Biomet, Inc. · 56 E Bell Dr · Warsaw, IN · 46582-6989
Is this the product you have?
- Knee Products
184762 Knees Vanguard Knee SystemSeries-A Standard Patella28 MM184764 Knees Vanguard Knee SystemSeries-A Standard Patella31
- MM Product UsageKnee prosthesis
- Lot codes and dates
- Lot Numbers
UDI Number 508390 Vanguard Knee SystemSeries-A Standard Patella28 MM (01)00880304431638(17)211218(10)508390309810 Vanguard Knee SystemSeries-A Standard Patella31 MM (01)00880304431317(17)211228(10)309810
- Lot Numbers
- Amount recalled
- 91 units
This recall covers 13 products
The agency filed one notice per product. You are reading one of them; the other 12 are below.
Where it was sold
- Nationwide
Why it was recalled
Potential presence of elevated endotoxin levels that exceed the specification limit
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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