Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055 Recalled by Biomet, Inc. Due to Product not properly being aligned with the adequate...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Biomet, Inc. directly.
Affected Products
Biomet ARTHROSIMPLICITY KIT EU Item Number: 24-4055
Quantity: 4 units OUS
Why Was This Recalled?
Product not properly being aligned with the adequate gamma sterilization group and result in the product not being properly sterilized
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Biomet, Inc.
Biomet, Inc. has 250 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report