570193 Platinum (drf)

Recall Summary Platinum (DRF) medical devices are being recalled in Canada due to safety or quality concerns that could affect patient health. The recall applies to all Platinum (DRF) devices distributed across Canada. This is classified as a Class I recall, which is the most serious type.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-12-13

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e7f15c9f-2e54-48c7-bf21-12062cf70fc0