3-way Latex Foley Catheter (2017-12-15)

3-Way Latex Foley Catheter Recall A 3-way latex Foley catheter is being recalled across Canada due to a medical device issue. The recall is classified as Class I, meaning there is a serious potential health risk. This product was distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-01-08

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e4448e27-291e-4e7b-86d3-7b0f51b27b17