# FDA recall Z-0295-2022

> **Medtronic Neuromodulation** · Class II · device recall initiated 2021-11-04.

## Product

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.

## 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

US Nationwide, including PR.  There was government distribution but no military distribution was identified.

## Key facts

- **Recall number:** Z-0295-2022
- **Recalling firm:** Medtronic Neuromodulation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-11-04
- **Report date:** 2021-12-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Minneapolis, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0295-2022

## Citation

> AI Analytics. FDA recall Z-0295-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0295-2022. Source: US FDA. Licensed CC0.

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