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Medtronic recalls embolization devices tied to 17 injuries, 4 deaths
Medtronic will remove one model of Pipeline Vantage devices from where they’re used and sold and will update the instructions ...
FDA classifies recall of Medtronic embolization devices as 'most serious'
The U.S. Food and Drug Administration on Tuesday classified the recall of Medtronic's embolization device as "most serious", ...
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TCAI becomes first US medical centre to use dual-energy ablation catheter
The Texas Cardiac Arrhythmia Institute (TCAI) at St David's Medical Center has become the first clinic in the US to use Medtronic ... indicates that the EP diagnostic catheter market will ...
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FDA tags Medtronic embolisation device recall as Class I
The US Food and Drug Administration (FDA) has tagged Medtronic’s recall of certain Pipeline Vantage embolisation devices as ...