FDAMay 3, 2024device

EVOLUTION¿ MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are for cemented use only.

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

microport orthopedicsmicroport

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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