Rtiset Blood Tubing Set (2021-01-05)

ARTISET Blood Tubing Set Recall Artiset blood tubing sets are being recalled across Canada due to a medical device issue. The recall is classified as Class I, which is the most serious type. The specific reason for the recall relates to a problem with the device itself, though details about the exact defect are not provided in this notice.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-01-15

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6f225906-8c6c-4cea-b61f-f5201925c33c