Aesculap Implant Systems LLC: Medical Device Recall in 2022 - (Recall #: Z-1410-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: October 25, 2021

Date Posted: July 27, 2022

Recall Number: Z-1410-2022

Event ID: 90544

Reason for Recall:

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

Status: Terminated

Product Quantity: 9 pieces

Code Information:

UDI-DI: 04046964067648

Distribution Pattern:

US: CA, FL, GA, IL, OH & MI

Voluntary or Mandated:

Voluntary: Firm initiated