Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
All instrumentation associated with the Prelude PF Resurfacing Knee System. Recalled by Biomet, Inc. Due to Inadequate design control.
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
All instrumentation associated with the Prelude PF Resurfacing Knee System.
Quantity: 576
Why Was This Recalled?
Inadequate design control.
Where Was This Sold?
This product was distributed to 12 states: CA, CO, GA, IN, KS, MI, MO, NJ, NC, OH, TN, TX
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