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

Recall Z-0700-2024 — VADER pedicle system, torque wrench, Catalog Number 42-702

U.S. FDA — Device Enforcement · Switzerland · 2023-11-28 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0700-2024
Date of alert
2023-11-28
Country / jurisdiction
Switzerland
Risk level
Class II
Risk type
recall
Brand
Icotec Ag
Product category
device
Product type
Devices
Reported risk: icotec has received notification of one revision that had to be carried out because nut screws had become loose. During the investigation of the device involved, it was detected that the torque limiting function of the wrench used to tighten the nut screws during implantation was not functioning correctly. Due to the malfunction, the nut screws may not have been tightened sufficiently.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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