Eli 380 Electrocardiograph (2015-05-29)

ELI 380 Electrocardiograph Recall Summary The ELI 380 Electrocardiograph device has been recalled across Canada due to a health products issue. This device is used to record heart electrical activity. The recall is classified as Class I, meaning there is a serious potential health risk associated with the device.

Reason

Health products

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-08-05

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0a1a08ef-b244-4fcb-9aff-94a18ec8b93c