Ngiography Pack (2019-10-25)

Angiography Pack Recall An Angiography Pack used in medical procedures has been recalled across Canada. The recall is classified as Class I, which is the most serious type, indicating the product could cause serious injury or death. The manufacturer has determined the device does not meet required medical standards.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-11-01

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e966de9e-e27d-4a06-bf0e-0bbb50b7bfd4