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FDA classifies recall of Medtronic embolization devices as 'most serious'

Signage is seen outside of FDA headquarters in White Oak, Maryland

Signage is seen outside of the Food and Drug Administration (FDA) headquarters in White Oak, Maryland, U.S., August 29, 2020. REUTERS/Andrew Kelly

 ANDREW KELLY

(Reuters) -The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", following reports of the deaths of four patients.

The use of the affected product could lead to severe adverse health consequences, including thrombosis, stroke, or death, the agency said.



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