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Aesculap Implant Systems LLC recalls MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441
Recalled July 27, 2022 · FDA recall Z-1410-2022 · Aesculap Implant Systems
Hazard
Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant. · FDA Class II
Units
9 pieces
Sold at
US: CA, FL, GA, IL, OH & MI
Description
Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.
Product
MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441
Manufacturer(s)
Aesculap Implant Systems LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →