Humidifier, Respiratory Gas, (Direct Patient Interface)
FDA product code BTT · Class 2 · 106 devices · 2,901 reports · 19 deaths reported · 6 devices named in recalls
- Airlife™ Sterile Water for Inhalation, USP, 500 ml 002620Airlife · Humidifier, Respiratory Gas, (Direct Patient Interface)1 report
- AirLife™ 377HTRAirlife · Humidifier, Respiratory Gas, (Direct Patient Interface)1 report
- AirLife™ AH290Airlife · Humidifier, Respiratory Gas, (Direct Patient Interface)1 report
- HUDSON RCI IPN049108Teleflex Incorporated · HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE)1 report
- HUDSON RCI IPN927526Teleflex Incorporated · HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE)1 report
- Portex 0552Icu Medical, Inc. · HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE)1 death1 report