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MicroPort Orthopedics Inc. recalls EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only
Recalled July 10, 2024 · FDA recall Z-2244-2024 · MicroPort Orthopedics
Hazard
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. · FDA Class II
Units
40 units
Sold at
International distribution in the country of China. There is no field inventory in the United States for either lot.
Description
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.
Product
EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.
Manufacturer(s)
MicroPort Orthopedics Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →