On June 11th, the @US_FDA identified a Class I Recall, the most serious type of recall: Edwards Lifesciences Recalls the IntraClude Intra-Aortic Occlusion Device Due to Risk of Balloon Rupture. Find out more are the recall: https://go.usa.gov/xy2tB   #FDA #MedicalDevicepic.twitter.com/2MwDtK3046

On June 11th, the @US_FDA identified a Class I Recall, the most serious type of recall: Edwards Lifesciences Recalls the IntraClude Intra-Aortic Occlusion Device Due to Risk of Balloon Rupture. Find out more are the recall: https://go.usa.gov/xy2tB  #FDA #MedicalDevice pic.twitter.com/2MwDtK3046

Source: Food and Drug Adminstration (FDA): CDRHNew - July 2, 2019 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news