Feather-flex Non-conductive Adult Anesthesia Circuit (2021-04-16)

Feather-Flex Non-Conductive Adult Anesthesia Circuit Recall Feather-Flex Non-Conductive Adult Anesthesia Circuits are being recalled across Canada because they are medical devices that do not meet safety standards. This recall affects anesthesia circuits used in hospitals and medical facilities. The recall was classified as Class I, indicating a serious safety concern.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-04-29

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/0b997ce8-c4d1-484f-972e-6f03ba672136