Mhi-tm2000 Linear Accelerator System (2017-12-05)

Recall Summary The MHI-TM2000 Linear Accelerator System is being recalled in Canada due to a medical device issue. This device is used in radiation therapy treatment. The recall affects all units distributed across Canada and has been classified as Class I, the most serious type of recall.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-12-21

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/345e33fc-c8ef-41c1-a2d4-328d311fd861