The FDA has issued a Class I recall of Medtronic’s Pipeline Vantage 027 embolization devices following reports of four patient deaths and 13 injuries associated with the devices. Read more at https://buff.ly/pVJCpvR by Ayesha Rashid about the recall of the devices, which are used to treat brain aneurysms. | Xtalks Webinars | Facebook
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Today, the FDA identified a Class I Recall, the most serious type of recall: Medtronic updated its 2019 recall of MiniMed 600 series insulin pumps to replace any MiniMed 600 series pump that has a clear retainer ring at no charge to customers. Find out more about this medical device recall. https://go.usa.gov/xMvAm | U.S. Food and Drug Administration
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