Reported Oct 14, 2020 · Terminated
Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055
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?
- Biomet
- ARTHROSIMPLICITY KIT EU Item Number24-4055
- Lot codes and dates
- Lot Numbers894660A 894660B 894670B 894700B
- Amount recalled
- 4 units OUS
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
Why it was recalled
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
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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