Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Various trauma and sports medicine instruments and implants. Spinal interlaminal Recalled by Biomet, Inc. Due to Insufficient seal strength on sterile barrier packaging. The...
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
Various trauma and sports medicine instruments and implants. Spinal interlaminal fixation orthosis.
Quantity: N/A
Why Was This Recalled?
Insufficient seal strength on sterile barrier packaging. The seal could be jeopardized causing the sterile barrier to be compromised and the product could become nonsterile. If the product becomes non-sterile and is used or implanted, it may lead to an infection.
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