Spectra Optia Apheresis (2019-05-21)

Spectra Optia Apheresis Recall Summary The Spectra Optia Apheresis medical device is being recalled across Canada. This is a Class I recall, which is the most serious category. The specific reason for the recall relates to a defect or safety concern with the device itself, though the details of the technical issue are not provided in this notice.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-06-14

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d80063fe-4c9b-4fd4-92ed-718929c1444d