FDA Device recall Z-2317-2024
GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
- FDA Device
- Class II
- ongoing
- Published 2024-07-17
On 2024-07-17 the FDA classified a Class II recall of GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW by Ge Vingmed Ultrasound As, citing 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….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2317-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-02 |
| Published | 2024-07-17 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Ge Vingmed Ultrasound As |
| Distribution | IL, MA, NM, NY, OK |
Product
GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
Reason
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.
Identifiers
| code_info | a) H45041SW, UDI/DI *, Serial Numbers: 001423S70 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2317-2024%22
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