Rrive, Braided Transseptal Sheath

Recall Summary Arrive Braided Transseptal Sheaths are being recalled in Canada because they may have defects in the braiding that could cause the device to break or separate during use. This device is used by doctors during certain heart procedures to access the heart tissue between its chambers.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-04-21

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fe9af675-d31f-4ee1-9f2d-1d3edaac8c88