Teleflex Disposable Aortic Punch (2020-01-14)

Teleflex Disposable Aortic Punch Recall Teleflex is recalling its Disposable Aortic Punch devices across Canada due to a defect in the medical device. The recall is classified as Class I, which indicates a serious health risk. This device is used in surgical procedures and may be affected regardless of where it was distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-01-31
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/5a288835-6b01-4511-9c11-73750469e00e