Every recall we track for AtriCure, Inc. — 7 in all — plus the complaints and injury reports the public filed about them.
AtriCure recalls tank hose assemblies with incorrect inner tube material and missing pin perforations. Affected units sold with specific product catalog number and lot number. Consumers should contact for remedy.
AtriCure recalls specific Cryo Module tank hose assemblies (product catalog A001053) due to incorrect material and missing pin perforations. Affected units may pose safety risks if used improperly.
AtriCure recalls EPi-Sense Guided Coagulation System with Visitrax model CDK-1413 due to potential compromised sterile package seal, which could lead to infection if used. Affected units include specific lots.
AtriCure recalls COBRA FUSION 50 Ablation System (Catalog # 700-002) due to potential elevated risk of TE in off-pump cardiac procedures without CPB. Affected units have UDI 00818354012811 and all lots within expiry.
AtriCure recalls COBRA FUSION 150 Ablation System (all lots) due to potential elevated risk of TE in off-pump cardiac procedures without CPB. Learn what to do.
AtriCure recalls COBRA FUSION 150 Ablation System (Catalog # 700-001S) due to potential elevated risk of TE during off-pump cardiac procedures. All units are affected.
AtriCure recalls its COBRA FUSION 150 Ablation System (International) due to potential elevated risk of thromboembolism in off-pump cardiac procedures without cardio pulmonary bypass.
