Fistula Wound Crown, Fistula Funnel, Isolator Strip (2019-01-25)

Recall Summary Three medical devices used in wound care—the Fistula Wound Crown, Fistula Funnel, and Isolator Strip—are being recalled across Canada. The recall was issued due to concerns with the devices themselves, classified as a serious safety issue. The devices were distributed nationwide in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-02-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/38a30121-d890-4a68-8454-fb3b4e955ffe