Reston Self-adhering Foam Pads (2019-05-07)

Reston Self-Adhering Foam Pads Recall Reston Self-Adhering Foam Pads are being recalled across Canada because they are classified as medical devices that do not meet regulatory requirements. This is a Class I recall, which indicates a serious health risk. The recall affects all Reston Self-Adhering Foam Pads distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-05-24
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/8851c7ca-85df-4b74-a8c8-671a121604ab