Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arcos Modular Revision Hip System Standard Cone Prox Body Recalled by Biomet, Inc. Due to Arcos Proximal Cone Bodies could potentially exhibit chatter...
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
Arcos Modular Revision Hip System Standard Cone Prox Body, Size B, 80 MM Item Number: 11-301342
Quantity: 12 units
Why Was This Recalled?
Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion and device failure in vivo leading to surgical intervention
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