FDAMarch 14, 2019device

Gridlock Ankle Screw Driver Bit REF 320-35-003 - Product Usage: A screwdriver facilitates implant insertion and removal.

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

The hazard

A screwdriver used to facilitate implant insertion and removal was found to be out of specification for the minor diameter of the drive feature causing the driver to be unable to retain screws as intended.

What to do

FDA enforcement status: Terminated

Brands named

trilliant surgicaltrilliant

UPCs

00812926026893

Recall history

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

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