Vivid 7 Dimension Ultrasound System, Vivid E9 Ultrasound System, Vivid E95 And Vivid E90 (2018-03-28)

GE Healthcare is recalling four ultrasound system models (Vivid 7 Dimension, Vivid E9, Vivid E95, and Vivid E90) that were distributed across Canada. The recall is classified as Class I, meaning there is a serious potential health risk associated with these devices. The specific reason for the recall relates to a medical device issue, though the details of the defect are not provided in this notice.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-04-24

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fa955fa1-8f96-4494-909a-4182d3fe5757