US FDA classifies recall of Inari’s catheter devices as ‘most serious’

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US FDA classifies recall of Inari’s catheter devices as ‘most serious’

(Reuters) – The U.S. Food and Drug Administration on Friday classified a recall of Inari Medical’s ClotTriever catheter that helps capture and remove large clot from big vessels as “most serious”. The affected products include all devices and lot numbers with labeled dates prior to Aug. 1, 2024, whose use might cause serious adverse health consequences, including device entrapment, vessel damage, and/or blockage of lung arteries and death, t…