Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement Recalled by MicroPort Orthopedics Inc. Due to One confirmed incident has been received that EFSRN4PR,...
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 MicroPort Orthopedics Inc. directly.
Affected Products
EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.
Quantity: 40 units
Why Was This Recalled?
One confirmed incident has been received that EFSRN4PR, lot number MP1982170, Size 4 Evolution MP Non-Porous Femoral Right was opened during surgery and contained part number EFSRN3PL, lot number MP1982097, Size 3 Evolution MP Non-Porous Femoral Left in the packaging.
Where Was This Sold?
International distribution in the country of China. There is no field inventory in the United States for either lot.
About MicroPort Orthopedics Inc.
MicroPort Orthopedics Inc. has 30 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report