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GE Vingmed Ultrasound As FDA Recalls

6 recalls on file across devices, 0 of them Class I and 6 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
GE Vivid Ultrasound products, Model Numbers: a) Vivid S70, H45041SWClass IIMay 2, 2024GE HealthCare has become aware of an issue with certain Vivi	GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Wo	Class IIDevices	May 2, 2024
GE Vivid Ultrasound products, Model Numbers: a) Vivid E90, H45581LB; b) Vivid E95, H45581DAClass IIMay 2, 2024GE HealthCare has become aware of an issue with certain Vivi	GE HealthCare has become aware of an issue with certain Vivid ultrasound systems where, due to a slow DICOM Wo	Class IIDevices	May 2, 2024
GE Healthcare Vivid S70, ultrasound deviceClass IIMay 30, 2023GE HealthCare has become aware that certain Vivid ultrasound	GE HealthCare has become aware that certain Vivid ultrasound systems cannot boot up in a timely fashion. If th	Class IIDevices	May 30, 2023
GE Healthcare Vivid S60N, ultrasound deviceClass IIMay 30, 2023GE HealthCare has become aware that certain Vivid ultrasound	GE HealthCare has become aware that certain Vivid ultrasound systems cannot boot up in a timely fashion. If th	Class IIDevices	May 30, 2023
GE Healthcare Vivid S70N, ultrasound deviceClass IIMay 30, 2023GE HealthCare has become aware that certain Vivid ultrasound	GE HealthCare has become aware that certain Vivid ultrasound systems cannot boot up in a timely fashion. If th	Class IIDevices	May 30, 2023
GE Healthcare Vivid S60, ultrasound deviceClass IIMay 30, 2023GE HealthCare has become aware that certain Vivid ultrasound	GE HealthCare has become aware that certain Vivid ultrasound systems cannot boot up in a timely fashion. If th	Class IIDevices	May 30, 2023

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