Reported Feb 8, 2023 · Ongoing
(1) Vanguard Knee System PS Open Box Femoral; Left; 57.5 mm. Intended for Knee joint replacement prostheses. Item…
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?
3 of 3 products
| Model / number | Product as published |
|---|---|
183122 | EXPANDED RECALL: (2) Vanguard Knee System PS Open Box Femoral; Left; 60 mm. |
183124 | (3) Vanguard Knee System PS Open Box Femoral; Left; 62.5 mm. |
183126 | — |
- Lot codes and dates
5 of 5 products
Products covered by this recall # Barcodes Product as published 1 008803042708620088030427087900880304270893(01)00880304270862(17)320504(10)J7186089 Lot Number: J7186089. Expanded Recall: (2)UDI: (01)00880304270879(17)320504(10)J7173870 Lot Number: J7173870. (3) UDI: (01)00880304270893(17)320504(10)J7192119 2 00880304270893(01)00880304270893(17)320504(10)J7197508 3 00880304270893(01)00880304270893(17)320504(10)J7209606 4 00880304270893(01)00880304270893(17)320504(10)J7220427 5 Lot Numbers: J7192119, J7197508, J7209606, J7220427 - Amount recalled
- 91 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
Why it was recalled
Components Incorrectly labeled as either smaller or larger and incorrect side (right/left).
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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