Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Active Articulation E1. Intended for use with either primary or Recalled by Biomet, Inc. Due to Biomet is recalling Active Articulation E1 Hip Bearing...
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
Active Articulation E1. Intended for use with either primary or revision hip arthroplasty.
Quantity: 8 units
Why Was This Recalled?
Biomet is recalling Active Articulation E1 Hip Bearing implants. Biomet has initiated this action following an investigation which identified that outer label indicates two conflicting O.D. sizes while the inner labels indicate an incorrect O.D. size. The implant itself is etched with the correct O.D. size.
Where Was This Sold?
Distributed in New York.
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