FDAOctober 25, 2021device

MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441

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

The hazard

Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.

What to do

FDA enforcement status: Terminated

Brands named

aesculap implant systemsaesculapaesculap implant

UPCs

04046964067648

Recall history

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

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