Philips Respironics Bipap And Humidifiers
Recall Summary Philips Respironics BiPAP and humidifier devices are being recalled across Canada due to performance issues. This recall affects BiPAP machines and associated humidifiers distributed throughout Canada. The FDA has classified this as a Class I recall, the most serious type.
- Product
- Philips Respironics BiPAP and Humidifiers
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-05-02
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/cd27c887-e012-4469-a40f-a981511f10d7