Pipeline Flex Embolization Device (2020-09-08)

Pipeline Flex Embolization Device Recall Summary The Pipeline Flex Embolization Device has been recalled across Canada. This device is used in medical procedures to treat certain blood vessel conditions in the brain. The recall affects patients who have received this device or healthcare facilities that have it in stock.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2020-10-02

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/4f0d28b5-5277-4f41-b327-7110ae516838