# FDA recall Z-0372-2025

> **Medtronic Neuromodulation** · Class II · device recall initiated 2024-09-18.

## Product

Medtronic Recharger Kits, RS6230,  RS7230, and RS5220A, containing components WR9230 and WR9220A Recharger for rechargeable implantable neurostimulators. The Rechargers are used with Neurostimulator Inceptiv INS Model 977119 and Percept RC INS Model B35300 as part of the Deep Brain Stimulation (DBS) system.  WR9220A is used with InterStim Micro, Model 97810, as part of Pelvic Health system

## Reason for recall

The Wireless Rechargers in the kits may be unable to enter a recharging session upon first use.

## Distribution

Worldwide - US Nationwide distribution in the states of AL, AZ, CA, FL, GA, ID, MD, MI, MN, MO, NC, NJ, OH, PA, SC, TX, VA, and WA. The countries of Austria, Belgium, Denmark, Finland, Germany, Ireland, Italy, Japan, Netherlands, Norway, Portugal, Spain, Sweden, Switzerland, and United Kingdom.

## Key facts

- **Recall number:** Z-0372-2025
- **Recalling firm:** Medtronic Neuromodulation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-09-18
- **Report date:** 2024-11-20

- **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-0372-2025

## Citation

> AI Analytics. FDA recall Z-0372-2025. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-0372-2025. Source: US FDA. Licensed CC0.

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