FDAJune 30, 2016device

PROFEMUR(R) MODULAR NECK, HIP FEMORAL NECK MicroPort total hip systems intended for use in total hip arthroplasty for reduction or relief of pain and/or improved hip function in skeletally mature patients.

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

The hazard

Profemur(R) neck, Item Number PHA01222 (Short AR VV2 Ti Neck) was labeled as Item Number PHA01212 (Short AR VV1 Ti Neck).

What to do

FDA enforcement status: Terminated

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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