Foot Control (2017-12-22)

Recall Summary A foot control device has been recalled across Canada due to issues classified as a Class I medical device recall. The specific details about what defect or safety concern prompted the recall are not provided in the information available. This recall affects all units distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-01-29

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0f75ca18-39be-4283-947f-275241d61784