K-act Kaolin Act Tubes (2020-11-09)

K-ACT Kaolin ACT Tubes Recall K-ACT Kaolin ACT Tubes are being recalled across Canada due to issues classified as a Class I medical device concern. The recall affects all K-ACT Kaolin ACT Tubes distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-11-27
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/fbd8582f-ba41-4ba4-a98f-336f145ab091