Spectra Optia Apheresis System (2019-07-19)

Spectra Optia Apheresis System Recall Summary The Spectra Optia Apheresis System, a medical device used to separate blood components, has been recalled in Canada. The recall is classified as Class I, meaning there is a serious potential health risk associated with the device. The device was distributed across Canada and may affect healthcare facilities and patients who have used or received treatment with this system.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-08-07

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c078277e-2f79-43ac-8183-93bf8963e6e8