FDAMay 2, 2024device
GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Ongoing
Brands named
ge vingmed ultrasound as
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- FDALumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,2025-10-31
- FDAPhilips S5-2 Ultrasound Transducer2025-09-05
- FDAPhilips Mini Multi TEE Ultrasound Transducer2025-09-05
- FDAPhilips OMNI III TEE Ultrasound Transducer2025-09-05
- FDAPhilips C9-4 Ultrasound Transducer2025-09-05
- FDAPhilips L17-5 Ultrasound Transducer2025-09-05
- FDAPhilips OMNI II TEE Ultrasound Transducer2025-09-05
- FDAPhilips 3D6-2 Ultrasound Transducer2025-09-05
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