On July 23rd, the @US_FDA identified a Class I Recall, the most serious type of recall: Datascope/Getinge Recalls Cardiosave Hybrid, Cardiosave Rescue, CS300 and CS100/100i Intra-Aortic Balloon Pumps. Find out more about the recall: https://go.usa.gov/xyANK   #MedicalDevicepic.twitter.com/dQRmsCdJ5x

On July 23rd, the @US_FDA identified a Class I Recall, the most serious type of recall: Datascope/Getinge Recalls Cardiosave Hybrid, Cardiosave Rescue, CS300 and CS100/100i Intra-Aortic Balloon Pumps. Find out more about the recall: https://go.usa.gov/xyANK  #MedicalDevice pic.twitter.com/dQRmsCdJ5x

Source: Food and Drug Adminstration (FDA): CDRHNew - July 25, 2019 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news