Kerlix 100% Bandage Cotton Large, Kerlix Amd Antimicrobial Large Roll, Dermacea Fluff Roll, And Kerlix Gauze Large Roll (2018-08-07)

Kerlix and DERMACEA gauze and bandage products in large roll sizes are being recalled across Canada due to issues classified as a Class I medical device recall. The specific reason for the recall relates to the products being classified as medical devices. This recall affects large roll versions of Kerlix 100% Bandage Cotton, Kerlix AMD Antimicrobial, DERMACEA Fluff Roll, and Kerlix Gauze products distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-10-19
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1d4a0804-5efe-4a8a-a26f-9db1cc7fb429