Z-0293-2022 Class II Ongoing
FDA device recall Z-0293-2022 was initiated by Medtronic Neuromodulation on Nov 4, 2021 and is designated Class II. Reason for recall: 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. The recall status is ongoing. Affected quantity: 10,081 devices.
Recall details
- Product Type
- Devices
- Report Date
- Dec 1, 2021
- Initiation Date
- Nov 4, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 10,081 devices
Product description
Medtronic Wireless Recharger Model WR9220 included in the RS5200 Recharger Kit used by the InterStim Micro (Model 97810) implantable neurostimulator.
Reason for recall
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.
Distribution pattern
US Nationwide, including PR. There was government distribution but no military distribution was identified.
Code information
UDI 00763000186265
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-0293-2022
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026