Reported Jun 12, 2019 · Terminated
Biomet Oxford Partial Knee Phase 3 / Domed Lateral Femoral Drill Guide: Item Number: 32-421930 System Domed Lateral…
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. · 1800 W Center St · Warsaw, IN · 46580-2304
Is this the product you have?
- Biomet Oxford Partial Knee Phase 3 /
- Domed Lateral Femoral Drill GuideItem
- Number32-421930 System Domed Lateral Femoral Drill Guide Small
- Lot codes and dates
- Lot NumbersZB160101 ZB160801 ZB160801
- Amount recalled
- 15
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
Why it was recalled
Incorrect raw material used by the supplier in the manufacturing of the screw component, which could potentially lead to corrosion.
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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