Capnostat 5 Mainstream Sensor Co2 Sensor, Respironics Loflo Sidestream Co2 Module (2019-02-28)
Recall Summary Philips is recalling CAPNOSTAT 5 mainstream CO2 sensors and Respironics LoFlo sidestream CO2 modules distributed across Canada. These devices are used to measure carbon dioxide levels during patient breathing and anesthesia. The recall was issued due to a device malfunction concern, though specific details about the malfunction are not provided in this notice.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-03-22
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/10cf820b-88d5-4bf5-ade4-ad62a78e4144