Ev Icd Pivotal Clinical Device (2020-08-13)

Recall Summary The EV ICD Pivotal Clinical Device is being recalled across Canada due to a medical device issue classified as Class I, meaning there is a serious potential health risk. The recall affects this implantable cardioverter-defibrillator device that was distributed nationwide in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-09-15
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/26da0172-5a7e-45dc-bbd5-f8bacdcaba3b