Flexible Shaft (2017-10-06)

Flexible Shaft Recall Summary A flexible shaft medical device is being recalled in Canada due to safety concerns. The device was distributed across Canada. This is classified as a Class I recall, which indicates a serious issue.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-10-13

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/82345bac-4d47-458c-ba6e-2e3e3285a87e