Maestro 4000 Cardiac Ablation System (2020-01-13)

Maestro 4000 Cardiac Ablation System Recall The Maestro 4000 Cardiac Ablation System is being recalled across Canada due to a medical device issue. This device is used in cardiac ablation procedures to treat certain heart rhythm problems. The recall is classified as Class I, meaning there is a potential for serious adverse health consequences.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-12-24
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f65d12ba-34a2-4b15-8e89-2f1f068b6cf7