Unlicensed Dynarex Products (2016-02-15)

Recall Summary Dynarex products distributed in Canada were recalled because they were unlicensed medical devices that did not meet regulatory requirements. The recall affected products distributed across Canada. This is a Class I recall, indicating a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-04-22

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ade9ba60-ab6c-4b6e-bd57-4d01119c2a51