# FDA recall Z-3073-2024

> **Medtronic Neuromodulation** · Class II · device recall initiated 2024-06-17.

## Product

Medtronic  Handset with Communicator, Model TH90Q01, InterStim Smart Programmer and Communicator Kits, containing the Model  HH90  Handset and the TM90 Communicator.

## Reason for recall

A subset of the handsets within the kit may not be able to complete the pairing process with the communicator upon initial setup.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-3073-2024
- **Recalling firm:** Medtronic Neuromodulation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-17
- **Report date:** 2024-09-18

- **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-3073-2024

## Citation

> AI Analytics. FDA recall Z-3073-2024. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-3073-2024. Source: US FDA. Licensed CC0.

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