Capnostream 20(p) And Battery Pack (2016-04-20)

Capnostream 20(p) and Battery Pack Recall Capnostream 20(p) capnography monitors and their battery packs distributed across Canada are being recalled. The devices are classified as a Class I recall, which indicates a serious issue with the medical device. This recall affects users of these monitoring devices in Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-04-27

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e566aa40-4263-4747-a4b7-9711cd594fb1