Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Edwards Lifesciences, LLC, Recalls SAPIEN 3 Ultra Delivery System Due to Burst Balloons During Surgery. Find out more about the recall: https://go.usa.gov/xV2Wm #MedicalDevicepic.twitter.com/Wo3BAbDGlF

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Edwards Lifesciences, LLC, Recalls SAPIEN 3 Ultra Delivery System Due to Burst Balloons During Surgery. Find out more about the recall: https://go.usa.gov/xV2Wm #MedicalDevice pic.twitter.com/Wo3BAbDGlF

https://twitter.com/FDADeviceInfo/status/1164643132484608007

Source: Food and Drug Adminstration (FDA): CDRHNew - August 22, 2019 Category: Medical Devices Authors: ( at FDADeviceInfo) Source Type: news

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