# FDA recall Z-2365-2023

> **Medtronic Neuromodulation** · Class II · device recall initiated 2023-07-06.

## Product

Medtronic InterStim Ground Pad REF 041826

## Reason for recall

Lot of InterStim Self-Adhesive Ground Pad is being recalled due to the product being labeled with the incorrect expiration date.

## Distribution

International distribution to the country of Iran.

## Key facts

- **Recall number:** Z-2365-2023
- **Recalling firm:** Medtronic Neuromodulation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-07-06
- **Report date:** 2023-08-16

- **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-2365-2023

## Citation

> MORVS. FDA recall Z-2365-2023. Retrieved 2026-10-16 from https://api.morvs.ai/recall/Z-2365-2023. Source: US FDA. Licensed CC0.

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