Maestro 4000 Cardiac Ablation System (2018-06-20)

MAESTRO 4000 Cardiac Ablation System Recall The MAESTRO 4000 Cardiac Ablation System is being recalled across Canada due to a medical device issue classified as Class I, the most serious type of recall. This device is used in heart procedures to treat abnormal heart rhythms. The recall affects all units of this system that were distributed in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2018-07-13
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a583033d-a922-4e8a-bd4b-02d4e04c5d1f