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GE Vingmed Ultrasound As recalls GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA
Recalled July 17, 2024 · FDA recall Z-2316-2024 · GE Vingmed Ultrasound As
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. · FDA Class II
Units
7 units
Sold at
US: IL, MA, NM, NY, OK,
Description
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.
Product
GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DA
Manufacturer(s)
GE Vingmed Ultrasound As
Made in
Norway
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →