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FDA Issues Early Alert About Risks of Peripheral Atherectomy Device

News Daily News

FDA Issues Early Alert About Risks of Peripheral Atherectomy Device

February 07, 2025

Label for Impella RP Flex Catheters Recalled to Address Anticoagulant Confusion: FDA

News Daily News

Label for Impella RP Flex Catheters Recalled to Address Anticoagulant Confusion: FDA

August 18, 2023

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

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Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

Michael O'Riordan

June 17, 2021

FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

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FDA: Penumbra JET 7 Clot Retrievers Recalled Following Deaths, Injuries

December 16, 2020

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

News Daily News

Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate

July 21, 2017

Catheter Kerfuffle: How Concerning Is Off-Label Use in Stroke Interventions?

News Features

Catheter Kerfuffle: How Concerning Is Off-Label Use in Stroke Interventions?

June 21, 2017

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