Cannulated Screw System

Cannulated Screw System Recall A Cannulated Screw System has been recalled across Canada because it is an unauthorized medical device that was not approved by Health Canada before being sold. This is a Class I recall, which means the device could potentially cause serious harm or death. The recall affects all Cannulated Screw System products distributed in Canada.

Product
Cannulated Screw System
Reason
Performance - Unauthorised device
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2023-03-15
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/41967286-20cf-42b2-9a7c-e32976a972b8