Flexitron Brachytherapy Remote Afterloading System (2019-11-20)

Flexitron Brachytherapy Remote Afterloading Systems are being recalled across Canada due to safety concerns with the medical device used in cancer radiation treatment. The recall is classified as Class I, meaning there is a serious risk of adverse health effects. This recall affects all units of this system that were distributed in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-11-29

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/465f150c-946c-4a79-96f8-de2daf1c4e35