FDAMay 22, 2017device

ECT Internal Fracture Fixation Drill 2.0 mm Diameter (.079 Inch), Item Number/EDI 00231802000, Nonsterile. orthopedic surgical instrument.

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

The hazard

Various trauma and extremity instruments (drill bits and screw taps) were manufactured from raw material with an anomaly. The anomaly may be on or below the surface and can increase the risk of instrument fracture.

What to do

FDA enforcement status: Terminated

Brands named

zimmer biometzimmer

UPCs

00231802000

Recall history

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

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