Mega2000 Patient Return Electrode

Mega2000 Patient Return Electrode Recall The Mega2000 Patient Return Electrode is being recalled in Canada due to a performance issue. This device is used in medical procedures to safely return electrical current from patients during certain treatments. The recall affects all Mega2000 Patient Return Electrodes distributed across Canada.

Product
Mega2000 Patient Return Electrode
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2024-06-26
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6ce12d7a-68bb-4917-93e1-b44dadc4e3f8