Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Medtronic Recalls Pipeline Flex Embolization Devices Due to Risk of Device Fracture.pic.twitter.com/Z271monZK1

Today, the @US_FDA identified a Class I Recall, the most serious type of recall: Medtronic Recalls Pipeline Flex Embolization Devices Due to Risk of Device Fracture. pic.twitter.com/Z271monZK1

https://twitter.com/FDADeviceInfo/status/1244722182380552194

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

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