Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Compress Face Reamer Product Usage: Correction of revision of unsuccessful Recalled by Biomet, Inc. Due to Investigation determined that units supplied were missing 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
Compress Face Reamer Product Usage: Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement, tumor resections, revision of previously failed total joint arthroplasty, and trauma.
Quantity: 4
Why Was This Recalled?
Investigation determined that units supplied were missing the 4x21 degree helix angle.
Where Was This Sold?
International Distribution in the countries of Netherlands, Europe, the Middle East, and Asia.
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