Profile Vortex Blue (2018-09-24)

ProFile Vortex Blue Recall Summary ProFile Vortex Blue devices are being recalled across Canada due to a medical device issue. The recall is classified as Class I, which is the most serious category. The devices were distributed nationwide in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-10-19

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d38fb6b5-f1b0-494a-a21e-2817d454e0c2