FDANovember 15, 2016device

Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory degenerative joint disease (NIDJD) or...

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

The hazard

All lots of modular neck hip prostheses are being recalled due to a higher than anticipated complaint and adverse event trend.

What to do

FDA enforcement status: Terminated

Brands named

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Recall history

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

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