Medtronic Pipeline Flex Embolization Device Receives an FDA Class I Recall After Two Reported Deaths The FDA has issued another Class I recall of Medtronic's Pipeline Flex embolization device after receiving reports of 59 malfunctions, ten severe injuries, and two fatalities. Medtronic Pipeline Flex Embolization Device is used … [Read more...] about Medtronic Pipeline Flex Embolization Device Wrongful Death Lawsuits