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

Recall Z-2353-2018 — microTargeting" Lead Adapter for microTargeting" Drive, Product Number 66-CN-DB

U.S. FDA — Device Enforcement · United States · 2018-05-10 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2353-2018
Date of alert
2018-05-10
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
FHC, Inc.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00873263004531
Reported risk: The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, and has resulted in the need to remove and replace the implanted lead intraoperative or in a follow-up procedure.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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