Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Teleflex Medical Recalls Comfort Flo Humidification Systems Due to Malfunction That May Cause Water to Enter Airway.pic.twitter.com/lbZJLpL8Wl

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Teleflex Medical Recalls Comfort Flo Humidification Systems Due to Malfunction That May Cause Water to Enter Airway. pic.twitter.com/lbZJLpL8Wl

Source: Food and Drug Adminstration (FDA): CDRHNew - February 19, 2020 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news