Pipeline Flex Embolization Device (2021-07-19)

Pipeline Flex Embolization Device Recall The Pipeline Flex Embolization Device has been recalled in Canada due to a medical device issue. This device is used in medical procedures and was distributed across Canada. The recall is classified as Class I, indicating a serious safety concern.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-07-27

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/eafd1ca2-b8c0-4f10-a4f3-58260c1f0eeb