Published on
February 19, 2020
- 19:20 GMT
Teleflex Medical Recalls Comfort Flo Humidification Systems Due to Malfunction That May Cause Water to Enter Airway
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Name and Version: COMFORT FLO Humidification System, REF 2410, Humidifier Nebulizer Kit Product …
Distribution channels:
Healthcare & Pharmaceuticals Industry
