Magnetom Vida And Sola (2019-06-09)

MAGNETOM Vida and Sola Recall Summary Siemens Healthineers has recalled MAGNETOM Vida and Sola magnetic resonance imaging (MRI) systems distributed across Canada due to a potential safety issue with the medical devices. This is a Class I recall, indicating a serious concern. The recall affects MRI systems that were distributed nationwide in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-06-21
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e2d20c82-7f15-4b57-9c29-02d7e44e2865