Carescape Monitor B650 (2018-05-31)

Carescape Monitor B650 Recall Summary The Carescape Monitor B650 medical device has been recalled across Canada due to unspecified safety concerns related to the device's functionality. This recall affects all units of this monitor that were distributed in Canada. The device is classified as a Class I recall, indicating a serious potential health risk.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-07-19

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/45bbaf1b-195b-407b-9641-20db933731c4