Zoll Aed Pro External Defibillator (2019-06-11)

ZOLL AED Pro External Defibrillator Recall ZOLL AED Pro defibrillators sold in Canada are being recalled because they may not deliver the correct electrical therapy to a patient's heart during use. This is a serious issue that affects the device's ability to function as intended in an emergency situation. The recall applies to devices distributed across Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-06-18

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c13c298f-6768-4c3b-9a6e-ca50a4cee346