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

Recall Z-0294-2022 — Medtronic Wireless Recharger Model WR9200 included in the RS6200 Recharger Kit used by the Activa RC (Model 37612) implantable neurostimulator.

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-0294-2022
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): 00763000185152

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

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.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-0294-2022 — Medtronic Wireless Recharger Model WR9200 included in the RS6200 Recharger Kit used by the Activa RC (Model 37612) implantable neurostimulator.

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