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

Recall Z-0295-2022 — Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger Kit used by the RestoreUltra (Model 37712), RestoreSensor (Model 37714), Restore Ultra SureScan MRI (Model 97712), and RestoreSensor SureScan MRI (Model 97714) implantable neurostimulators.

U.S. FDA — Device Enforcement · United States · 2021-11-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0295-2022
Date of alert
2021-11-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medtronic Neuromodulation
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00763000217921
Reported risk: The wireless rechargers (WR; WR9200 and WR9220; included in the Recharger Kits) become unresponsive if the charging steps, indicated in the Recharger Patient User Guide, are not followed.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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