On August 12th, the @US_FDA identified a Class I Recall, the most serious type of recall: Fresenius Kabi Recalls Volumat MC Agilia Infusion Pump and Vigilant Agilia Drug Library. Find out more about the recall: https://go.usa.gov/xVCyk   #MedicalDevicepic.twitter.com/vfFRY5a3aw

On August 12th, the @US_FDA identified a Class I Recall, the most serious type of recall: Fresenius Kabi Recalls Volumat MC Agilia Infusion Pump and Vigilant Agilia Drug Library. Find out more about the recall: https://go.usa.gov/xVCyk  #MedicalDevice pic.twitter.com/vfFRY5a3aw

Source: Food and Drug Adminstration (FDA): CDRHNew - August 16, 2019 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news