Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Knee Products: TMJPM-1510 Microfixation Custom Made Device Recalled by Biomet, Inc. Due to Potential presence of elevated endotoxin levels that exceed...
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
Knee Products: TMJPM-1510 Microfixation Custom Made Device, Left PM-TMJ Model (01)00841036226534(17)220111(10)735550 Product Usage: Knee prosthesis
Quantity: 1
Why Was This Recalled?
Potential presence of elevated endotoxin levels that exceed the specification limit
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