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GE Vingmed Ultrasound As Recall 92505

Description: GE Healthcare Vivid S60N, ultrasound device

GE Vingmed Ultrasound As Recall 92505 Information

Mandated?Voluntary: Firm initiated
Recall NumberZ-2126-2023
Event ID92505
Event DescriptionGE Healthcare Vivid S60N, ultrasound device
Product TypeDevices
DistributionWorldwide distribution.
Recall ReasonGE HealthCare has become aware that certain Vivid ultrasound systems cannot boot up in a timely fashion. If this occurs, it can delay availability of the device in time-critical emergency situations.
Device Classification20230719
Device Code InfoSoftware versions: v203, v204, v205, v206
Center Classification Date20230710
Recall Initiation Date20230530
Recalling FirmGE Vingmed Ultrasound As
Initial Notification Letter
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