Torflex Transseptal Guiding Sheath (2019-10-08)

Recall Summary TorFlex Transseptal Guiding Sheath devices are being recalled across Canada due to a medical device issue. The recall is classified as Class I, meaning there is a serious potential health risk associated with the product. These devices were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-11-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b231c441-1556-4652-a96c-3f5df03522b4