Magnetom Sola (2020-02-27)

MAGNETOM Sola Recall Summary The MAGNETOM Sola MRI machine is being recalled across Canada due to a medical device issue. This recall affects healthcare facilities that use this equipment. The FDA has classified this as a Class I recall, which is the most serious classification.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-03-13
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/34534308-15b0-4d22-a038-dba574dde503