Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA is listed as a material on 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
Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm, and 17mm
Quantity: 21
Why Was This Recalled?
PMMA is listed as a material on the label but the product does not contain PMMA.
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