Atricure, Inc.
Mason, OH
This page shows every FDA and USDA recall linked to Atricure, Inc.. Each entry includes the product involved, when the recall happened, and how serious it was. If a company has had multiple recalls over the years, you can see the full history here in one place — including whether any were Class I, which is the most serious type.
10
Total Recalls
2016
First Recall
2024
Most Recent
Packaged, Tank Hose Assembly CMA-US, Product Catalog Number A001056
Jan 31, 2024
· Device
Active
Cryo Module Accessories Domestic CMA-OUS, Product Catalog Number A001053
Jan 31, 2024
· Device
Active
EPi-Sense Guided Coagulation System with Visitrax, MOdel No. CDK-1413 - Product Usage: The EPi-Sense Guided Co...
May 29, 2019
· Device
Terminated
COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001S
Jan 22, 2019
· Device
Terminated
COBRA FUSION 150 Ablation System, Catalog # (REF) 700-001
Jan 22, 2019
· Device
Terminated
COBRA FUSION 150 Ablation System (International Only), Catalog # (REF) 700-001MI
Jan 22, 2019
· Device
Terminated
COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002
Jan 22, 2019
· Device
Terminated
AtriClip" LAA Exclusion System with preloaded Gillinov-Cosgrove" Clip - A single PRO2 device is packaged in a...
Nov 30, 2016
· Device
Terminated
COBRA Fusion 50 Ablation System, COBRA Fusion 150 Ablation System, and COBRA Fusion Magnetic Retriever System....
Sep 22, 2016
· Device
Terminated
AtriClip LAA Exclusion System with preloaded Gillinov-Cosgrove Clip
Product is used for the occlusion of the h...
Sep 22, 2016
· Device
Terminated