Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1410-2022 — MODULIFT VBR SZ.M 4MM SET SCREW DRIVER, MF790R, part of Modulift VBR Medium Instrument Set, ST-0441

U.S. FDA — Device Enforcement · United States · 2021-10-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1410-2022
Date of alert
2021-10-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Aesculap Implant Systems LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
04046964067648
Reported risk: Set screwdriver fails during surgery by deforming at the tip during engagement and manipulation of the implant.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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