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November

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Month: November 2020

medical device recall
By mclineIn Medical Device RecallPosted November 4, 2020

FDA Issues Class I Medical Device Recall for Medtronic Septostomy Catheters

The U.S. Food and Drug Administration (FDA) is categorizing Medtronic’s septostomy catheter recall as Class I.  A Class I medical device recall is the most serious, meaning that use of the medical device could cause serious injuries or death.  Here is what we know about the recall. Medical Device Recall...

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