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FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

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FDA: Class I Recall for Medtronic’s 6-Fr Sherpa NX Guide Catheter

Michael O'Riordan

October 09, 2019

Terumo’s Solopath Transfemoral System and Recollapsible Balloon Access System Recalled for Dislodging Issues

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Terumo’s Solopath Transfemoral System and Recollapsible Balloon Access System Recalled for Dislodging Issues

May 30, 2019

Patients Retain Little From Cath Lab Informed-Consent Conversations

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Patients Retain Little From Cath Lab Informed-Consent Conversations

Michael O'Riordan

April 26, 2019

News Daily News

Abbott to Issue Urgent Recall of Certain Lots of Vascular Closure System

February 10, 2017

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Use of Smaller Catheters in Radial PCI Cuts Access-Site Complications

April 15, 2014

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