Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Medtronic Recalls HeartWare HVAD Pump Outflow Graft and Outflow Graft Strain Relief Due to Risk of Breaks and Tears During Set Up.pic.twitter.com/m68O7tKrDG

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Medtronic Recalls HeartWare HVAD Pump Outflow Graft and Outflow Graft Strain Relief Due to Risk of Breaks and Tears During Set Up. pic.twitter.com/m68O7tKrDG

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