# FDA recall Z-1938-2025

> **GE Medical Systems Information Technologies Inc** · Class II · device recall initiated 2025-04-25.

## Product

MUSE 5 Systems, Model Numbers 2021274-001, 2023032-005, 2027478-001, Large capacity client-server-based computer system that accesses stores and manages cardiovascular information.

## Reason for recall

The MUSE Administrator Account active directory or local credential could potentially be used from your local network to log into a GE HealthCare MUSE 5 system and potentially manipulate recorded patient data.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-1938-2025
- **Recalling firm:** GE Medical Systems Information Technologies Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-25
- **Report date:** 2025-06-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Milwaukee, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1938-2025

## Citation

> AI Analytics. FDA recall Z-1938-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1938-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*