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Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

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Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

Yael L. Maxwell

April 03, 2024

FDA Alerts Doctors to Potential Late Risks With Paclitaxel-Coated Balloons and Stents in PAD

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FDA Alerts Doctors to Potential Late Risks With Paclitaxel-Coated Balloons and Stents in PAD

Michael O'Riordan

January 17, 2019

FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

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FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

October 16, 2018

FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

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FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

October 02, 2017

News Daily News

FDA Announces Recall of Bard’s Halo One Peripheral Vascular Guiding Sheath

January 31, 2017

News Daily News

FDA: Vascu-Guard Patch Associated With Bleeding, Death After Carotid Endarterectomy

Yael L. Maxwell

September 02, 2016

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