PlainRecalls
FDA Devices Moderate Class II Terminated

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

Reported: July 27, 2022 Initiated: October 25, 2021 #Z-1410-2022

Product Description

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

Reason for Recall

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

Details

Units Affected
9 pieces
Distribution
US: CA, FL, GA, IL, OH & MI
Location
Center Valley, PA

Frequently Asked Questions

What product was recalled?
MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441. Recalled by Aesculap Implant Systems LLC. Units affected: 9 pieces.
Why was this product recalled?
Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 27, 2022. Severity: Moderate. Recall number: Z-1410-2022.