Medtronic Spinous Process Clamp

Medtronic Spinous Process Clamp Recall Medtronic is recalling Spinous Process Clamps used in spinal surgery across Canada due to a manufacturing defect that could cause the clamp to fail and not properly secure the spinal implant. This recall affects medical facilities and hospitals that have received these devices. The clamps were distributed nationwide in Canada.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-09-05

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a47fb97f-48ca-471b-91d4-0bb769bc6f44