Mylab 70 X Vision And Xvg, Mylab Twice And Class C (2018-01-22)

Recall Summary MyLab ultrasound devices (MyLab 70 X Vision, MyLab XVG, MyLab Twice, and Class C models) are being recalled across Canada due to a medical device issue. The recall is classified as Class I, which indicates a serious safety concern. This affects all MyLab ultrasound systems of these models that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-03-13
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/48fb3011-c0b6-4c94-9dec-108245f9f77e