Cognis Cardiac Defibrillators (n106 And N107) And Teligen Implantable Defibrillators (n102 And E110) (2013-08-29)

Recall Summary Cognis and Teligen brand implantable defibrillators are being recalled across Canada due to a defect in the device. The affected models are Cognis N106 and N107, and Teligen N102 and E110. This is classified as a Class I recall, the most serious type, because the devices may fail to deliver therapy when needed.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2014-03-19

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/3ac70021-492e-447f-8dbd-de502da08f3c