Bis Complete Monitoring System (2018-07-26)

BIS Complete Monitoring System Recall The BIS Complete Monitoring System, a medical device used for patient monitoring, has been recalled across Canada. The device was recalled due to safety concerns related to how it functions as a medical device. This recall affects all units of this system that were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-08-17

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1d25ae7f-4a6c-4aff-8dea-d676d0b4d888