Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Teleflex Recalls the Galemed http://Babi.Plus   Pressure Relief Manifolds Due to Dislodged Valve.pic.twitter.com/Whzh0vrLa9

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Teleflex Recalls the Galemed http://Babi.Plus  Pressure Relief Manifolds Due to Dislodged Valve. pic.twitter.com/Whzh0vrLa9

Source: Food and Drug Adminstration (FDA): CDRHNew - January 28, 2020 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news