Sigma Spectrum Infusion System (v8 Platform) (2020-11-26)

SIGMA SPECTRUM Infusion System Recall SIGMA SPECTRUM Infusion System devices using the V8 Platform are being recalled across Canada. The recall was issued because the devices do not meet required safety and performance standards for medical devices. This recall affects SIGMA SPECTRUM infusion systems that were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-12-11
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e84fa655-3939-4fde-8da8-9cb17ce30d98