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XTANT Medical recalls Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591
Recalled July 15, 2020 · FDA recall Z-2500-2020 · XTANT Medical
Hazard
The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld. · FDA Class II
Units
4 units
Sold at
AZ, TX and WV.
Description
The strike plate fractured off from the forceps inserter devices with minimal impaction or force due to unsatisfactory weld.
Product
Irix-C Forceps Inserter; Product Code/UDI: T066-0059/ M697T06600591
Manufacturer(s)
XTANT Medical
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →