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  • Dispositivo 3821
  • Fabricante 31827
  • Evento 4589
  • Implante 424
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Cidex General Hospital and Personal Use Devices Advanced Sterilization Products United States USFDA
Device Recall Cidex General Hospital and Personal Use Devices Advanced Sterilization Products United States USFDA
Easypump LT 60-24 || Easypump Infusion Pump (60 ml x 2 ml/hr) General Hospital and Personal Use Devices I-Flow Corporation United States USFDA
Titanium Dual Lumen Implantable Port with PASV Valve and 10F Silicone Catheter. Catalog No/REF: PRTB10A, Model No. M001PRTB10A. Firm on label: Boston Scientific Corp., NAMIC Technology Center, Glens Falls, NY 12801. General Hospital and Personal Use Devices Boston Scientific Corporation United States USFDA
Device Recall BardPort Titanium Implanted Port. General Hospital and Personal Use Devices Bard Access Systems United States USFDA
Portex General Hospital and Personal Use Devices Smiths Medical ASD, Inc. United States USFDA
Device Recall Richard Wolf Medical Instrument Corp. ICart General Hospital and Personal Use Devices Richard Wolf Medical Instruments Corp. 1 United States USFDA
Device Recall HillRom Liko General Hospital and Personal Use Devices Hill-Rom, Inc. 1 United States USFDA
Device Recall P440 Portable Lift General Hospital and Personal Use Devices ErgoSafe Products, LLC (DBA) Prism Medical 1 United States USFDA
Device Recall P600 Portable Lift General Hospital and Personal Use Devices ErgoSafe Products, LLC (DBA) Prism Medical 1 United States USFDA
Device Recall Tray, irrigation, sterile General Hospital and Personal Use Devices Customed, Inc 1 United States USFDA
Device Recall CURATION KIT General Hospital and Personal Use Devices Customed, Inc 1 United States USFDA
Device Recall Lite DM (Lite Data Manager) General Hospital and Personal Use Devices Horiba Instruments Inc 1 United States USFDA
Device Recall CIVCO Shoulder Retractors General Hospital and Personal Use Devices Med Tec Inc 1 United States USFDA
Device Recall Regard General Hospital and Personal Use Devices Resource Optimization & Innovation Llc 1 United States USFDA
Device Recall Regard General Hospital and Personal Use Devices Resource Optimization & Innovation Llc 1 United States USFDA
Device Recall Regard General Hospital and Personal Use Devices Resource Optimization & Innovation Llc 1 United States USFDA
Device Recall Regard General Hospital and Personal Use Devices Resource Optimization & Innovation Llc 1 United States USFDA
Device Recall Regard General Hospital and Personal Use Devices Resource Optimization & Innovation Llc 1 United States USFDA
Device Recall MicroScan LabPro Information Manager System General Hospital and Personal Use Devices Beckman Coulter Inc. 1 United States USFDA
Device Recall Baxter SelfRighting Luer Lock Tip Cap General Hospital and Personal Use Devices Baxter Corporation Englewood 1 United States USFDA
Device Recall CIVCO Medical Solutions General Hospital and Personal Use Devices Med Tec Inc 1 United States USFDA
Device Recall CIVCO Medical Solutions General Hospital and Personal Use Devices Med Tec Inc 1 United States USFDA
Device Recall Baxter General Hospital and Personal Use Devices Baxter Corporation Englewood 1 United States USFDA
Device Recall Puritan absorbent foam tipped applicator General Hospital and Personal Use Devices Puritan Medical Products Co., LLC 1 United States USFDA
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Aviso

Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.