Class II
Medical Device Recall: GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SW
GE Vingmed Ultrasound As · May 2, 2024
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.
Distribution
US: IL, MA, NM, NY, OK,
States Affected
IL, MA, NM, NY, OK
Quantity Affected
1 unit
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2317-2024
Status: ongoing
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