Schanz Screw Self Drill (2017-09-19)

Schanz Screw Self Drill Recall Summary Schanz Screw Self Drill medical devices are being recalled across Canada due to a safety concern with the devices themselves. This recall affects all Schanz Screw Self Drill products that were distributed in Canada. The devices are classified as a Class I recall, which is the most serious type.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-10-05
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e986ff07-b4a1-4c70-a087-3618731d2a40