FDAMay 12, 2020device

Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591

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

The hazard

The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld.

What to do

FDA enforcement status: Terminated

Brands named

xtant medicalxtant

Recall history

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

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