Sicd System Pulse Generators (2017-07-04)

Recall Summary Certain SICD (subcutaneous implantable cardioverter-defibrillator) System pulse generators distributed across Canada are being recalled due to a medical device issue. The recall affects patients who have received these devices. This is classified as a Class I recall, which is the most serious category.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-07-17

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/9284c502-d647-4b3f-8f73-c6a45d32df80