Cardiovit At-102 Plus

Cardiovit AT-102 Plus Recall Summary The Cardiovit AT-102 Plus electrocardiogram (ECG) device is being recalled in Canada due to a medical device issue. This device was distributed across Canada and is used to record heart electrical activity. The recall is classified as Class I, indicating a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-02-09

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e228ca28-c932-4787-a777-0292db8e189a