FDA Device recall Z-2125-2023
GE Healthcare Vivid S70, ultrasound device
- FDA Device
- Class II
- ongoing
- Published 2023-07-19
On 2023-07-19 the FDA classified a Class II recall of GE Healthcare Vivid S70, ultrasound device by Ge Vingmed Ultrasound As, citing 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 e….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2125-2023 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-05-30 |
| Published | 2023-07-19 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Ge Vingmed Ultrasound As |
| Distribution | n/a |
Product
GE Healthcare Vivid S70, ultrasound device
Reason
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.
Identifiers
| code_info | Software versions: V203, v204 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2125-2023%22
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