# FDA recall Z-2226-2023

> **Medtronic Neuromodulation** · Class II · device recall initiated 2023-06-21.

## Product

A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..

## Reason for recall

When an update to the A710 Clinician Programmer software application for the Intellis Neurostimulation System was released, the corresponding version of the A901 Communication Manager software application was not available for download.

## Distribution

International distribution to the countries of Israel and Serbia.

## Key facts

- **Recall number:** Z-2226-2023
- **Recalling firm:** Medtronic Neuromodulation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-06-21
- **Report date:** 2023-08-02

- **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-2226-2023

## Citation

> AI Analytics. FDA recall Z-2226-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2226-2023. Source: US FDA. Licensed CC0.

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