Sicd System - Q-tech Programmer (2017-07-04)

Recall Summary Q-Tech Programmer devices used with SICD (subcutaneous implantable cardioverter-defibrillator) systems are being recalled across Canada due to a medical device issue. This recall affects patients who have received these programmers as part of their SICD system. The recall is classified as Class I, indicating a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-11-24

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/83a3ac02-494e-42c5-8459-ccc4e2b79529