FDAOctober 29, 2024device

EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEMORAL COMPONENT CS/CR NON-POROUS SIZE 6 LEFT PRIMARY, REF: EFSRN6PL Knee prosthesis component

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

The hazard

Femoral implant porous size 5 right primary and femoral implant non-porous size 6 left primary have correct markings on devices, but may have incorrect 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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