FDAFDA · Food and drugs·Recall number Z-0081-2021
Biomet Regenerex Primary Taper Cap Item Number 141269
Published October 14, 2020 · Recall initiated: September 4, 2020
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Biomet, Inc.
- Distributor
- Nationwide Foreign: Canada, FINLAND, NETHERLANDS, UNITED KINGDOM
- Lot
- Lot Numbers: 015800 324440 685300 023900 324440R 696280 058930 389060 821980 200720 418430 890320 313260 646040 997610
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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