Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Biomet 8.0 Cannulated Screw Tap-Bone fixation screw Item Number: 110008467 Recalled by Biomet Due to Distributed to the field without having completed design...
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 directly.
Affected Products
Biomet 8.0 Cannulated Screw Tap-Bone fixation screw Item Number: 110008467 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
Quantity: 10 OUS
Why Was This Recalled?
Distributed to the field without having completed design history files or design transfer activities
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Biomet
Biomet has 24 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report