Spectra Optia Apheresis System - Main Uni

Recall Summary Spectra Optia Apheresis System main units are being recalled in Canada because they may not function properly during blood collection procedures due to a potential software issue. The recall affects medical facilities across Canada that use this equipment. [No further details on affected serial numbers or specific patient impact are provided in the information given.]

Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-06-07
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/16cecb36-4afe-462c-9ed1-bd75b26d7770