AtriCure, Inc. recalls

11 recalls on record · latest: November 28, 2023

Official U.S. recall history for AtriCure, Inc., compiled from official government records.

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AtriCure, Inc. recalls Cryo Module Accessories Domestic CMA-OUS, Product Catalog Number A001053

November 28, 2023 · Medical device recalls Moderate risk AtriCure has identified certain lots of tank hose assemblies where a second-tie…

AtriCure, Inc. recalls Packaged, Tank Hose Assembly CMA-US, Product Catalog Number A001056

November 28, 2023 · Medical device recalls Moderate risk AtriCure has identified certain lots of tank hose assemblies where a second-tie…

EPi-Sense Guided Coagulation System with Visitrax recalled over sterility concerns

May 29, 2019 · Medical device recalls Moderate risk The sterile package seal for the Epi-Sense Guided Coagulation System may be com…

AtriCure, Inc. recalls COBRA FUSION 150 Ablation System (International Only), Catalog # (REF) 700-001MI

January 22, 2019 · Medical device recalls Moderate risk There is a potential for patients undergoing ablation to experience an elevated…

AtriCure, Inc. recalls COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001S

January 22, 2019 · Medical device recalls Moderate risk There is a potential for patients undergoing ablation to experience an elevated…

AtriCure, Inc. recalls COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001

January 22, 2019 · Medical device recalls Moderate risk There is a potential for patients undergoing ablation to experience an elevated…

AtriCure, Inc. recalls COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002

January 22, 2019 · Medical device recalls Moderate risk There is a potential for patients undergoing ablation to experience an elevated…

AtriCure, Inc. recalls AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a conventio…

November 30, 2016 · Medical device recalls Moderate risk A complaint of the PRO2 jaw breaking prior to surgery being performed.

AtriCure, Inc. recalls AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip Product is used for the occlusion of the heart's le…

September 22, 2016 · Medical device recalls Moderate risk There is a potential for a component failure of the device which could necessit…

AtriCure, Inc. recalls COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System. Model Nu…

September 22, 2016 · Medical device recalls Moderate risk Due to product design and process control, part of the device can separate and…

Atricure Inc recalls Cryogenic probe for cardiac ablation surgery, packaged individually in Tyvek pouches Product Usage: Cryogenic probe for…

November 21, 2014 · Medical device recalls Moderate risk Affected product may have compromised sterility due to packaging defects. It wa…