Today, the @US_FDA identified a Class I Recall, the most serious type of recall: CME America Recalls CME America BodyGuard Infusion Pump System Due to Risk of Over- and Under-Infusionpic.twitter.com/YyHeC3URXT

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: CME America Recalls CME America BodyGuard Infusion Pump System Due to Risk of Over- and Under-Infusion pic.twitter.com/YyHeC3URXT

Source: Food and Drug Adminstration (FDA): CDRHNew - March 30, 2020 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news