On August 5th, the @US_FDA identified a Class I Recall, the most serious type of recall: Abbott recalls Ellipse Implantable Cardioverter Defibrillators due to exposed aluminum wires. Find out more about the recall: https://go.usa.gov/xySzm #MedicalDevicepic.twitter.com/3Vsug4KRKB
On August 5th, the @US_FDA identified a Class I Recall, the most serious type of recall: Abbott recalls Ellipse Implantable Cardioverter Defibrillators due to exposed aluminum wires. Find out more about the recall: https://go.usa.gov/xySzm #MedicalDevice pic.twitter.com/3Vsug4KRKB
Source: Food and Drug Adminstration (FDA): CDRHNew - Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news