Medtronic Deep Brain Stimulation (dbs) Lead Kits (2017-03-23)

Medtronic DBS Lead Kits Recall Medtronic is recalling deep brain stimulation lead kits used in neurosurgery procedures across Canada due to a manufacturing defect that could cause the leads to fail or malfunction. The defect affects kits distributed from 2017 onward. This recall impacts patients who have received or may receive these DBS devices, as well as healthcare facilities that use them.

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-03-23

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/8472691b-488e-4799-8846-7628fb51f59f