GE Vivid Ultrasound products — Class II medical device recall Z-2317-2024
Ongoing recall by GE Vingmed Ultrasound As, reported 2024-07-17, distributed in IL, MA, NM, NY, OK. GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Wo
| Recall number | Z-2317-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Vingmed Ultrasound As, Horten, N/A, Norway |
| Recall initiated | 2024-05-02 |
| Classified | 2024-07-05 |
| Reported by FDA | 2024-07-17 |
| Distributed | IL, MA, NM, NY, OK |
| Quantity | 1 units |
| Serial numbers | 001423S70 |
Product
GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2317-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.