Hoffmann Lrf-hinge Coupling (2018-03-02)

Hoffmann LRF-Hinge Coupling Recall Summary Hoffmann LRF-Hinge Coupling medical devices are being recalled across Canada due to a safety concern. The devices are classified as a Class I recall, meaning there is a serious risk of adverse health effects. This recall affects all Hoffmann LRF-Hinge Coupling devices distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-04-03
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/012d80a1-44d3-4ad3-88b8-d683ca11c0b0