Modern Healthcare5d
FDA deems Medtronic’s Pipeline Vantage recall ‘most serious’
The recall, which affects two models of Pipeline Vantage embolization devices, is linked to 17 injuries and four deaths.
MedTech Dive5d
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 ...
MassDevice6d
Medtronic recalls embolization device after reported deaths
The FDA deemed a recall of some Medtronic Pipeline Vantage embolization devices serious after multiple deaths related to the ...
Hosted on MSN10mon
Medtronic (MDT) Reports Favorable SPHERE Per-AF Trial Outcome
Medtronic’s Sphere-9 Catheter is an all-in-one pulsed field ... As pioneers in cardiac ablation treatment, including cryoablation and PFA, the company is thrilled to share these results ...
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", ...
Hosted on MSN3mon
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’s Affera mapping and ablation system with the Sphere-9 catheter ...
Yahoo Finance1mon
Boston Scientific bags CE marking for Farapulse catheter and software
“The Farawave NAV Ablation Catheter and Faraview software ... According to GlobalData analysis, since the FDA approval of Medtronic’s PulseSelect PFA system in December 2021 and Boston ...