# FDA recall Z-2124-2023

> **GE Vingmed Ultrasound As** · Class II · device recall initiated 2023-05-30.

## Product

GE Healthcare Vivid S60, ultrasound device

## Reason for recall

GE HealthCare has become aware that certain Vivid ultrasound systems cannot boot up in a timely fashion. If this occurs, it can delay availability of the device in time-critical emergency situations.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-2124-2023
- **Recalling firm:** GE Vingmed Ultrasound As
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-30
- **Report date:** 2023-07-19

- **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-2124-2023

## Citation

> AI Analytics. FDA recall Z-2124-2023. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-2124-2023. Source: US FDA. Licensed CC0.

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