Fred Easyport (2019-04-13)

Summary FRED easyport devices distributed across Canada are being recalled due to a medical device issue. The recall is classified as Class I, meaning there is a serious potential health risk associated with the product. The recall affects all Canadian consumers who have this device.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-05-14

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/69d9882c-b227-45f0-982a-d8505040b8d9