FDAApril 28, 2010device

AperFix Femoral Implant Coring Removal Drill, labeled as the following: a. Femoral Removal Coring Reamer 9mm, Model Number CM-7109; b. Femoral Removal Coring Reamer 10mm, Model Number CM-7110; c. Femoral Removal Coring Reamer 11mm, Model Number CM-7111; d. Femoral Removal Coring Reamer 9 mm - Lon...

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

The hazard

A review of product complaints in 2010 identified a trend for the Coring Removal Drill of premature wear and/or breakage. This recall occurred in 2013.

What to do

FDA enforcement status: Terminated

Brands named

cayenne medicalcayenne

Recall history

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

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