# FDA recall Z-2316-2024

> **GE Vingmed Ultrasound As** · Class II · device recall initiated 2024-05-02.

## Product

GE Vivid Ultrasound products, Model Numbers:    a) Vivid E90, H45581LB;   b) Vivid E95, H45581DA

## Reason for recall

GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Worklist response time, incorrect patient name and demographics can be displayed on the ultrasound scanner screen rather than the intended patient selected by the user.

## Distribution

US:  IL, MA, NM, NY, OK,

## Key facts

- **Recall number:** Z-2316-2024
- **Recalling firm:** GE Vingmed Ultrasound As
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-02
- **Report date:** 2024-07-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Horten, N/A, Norway

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2316-2024

## Citation

> AI Analytics. FDA recall Z-2316-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2316-2024. Source: US FDA. Licensed CC0.

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