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  • Dispositivo 190
  • Fabricante 67
  • Evento 124969
  • Implante 4
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Churchill Medical General and Plastic Surgery Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Churchill Medical 78" Stopcock Extension Set General Hospital and Personal Use Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Churchill Medical Systems 14"Extension Set General Hospital and Personal Use Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Churchill Medical Systems 6" Microbore Trifurcated General Hospital and Personal Use Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Churchill Medical Systems Central Line and Port Dressing Kit General Hospital and Personal Use Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Churchill Medical Systems Central Line Dressing Kit General Hospital and Personal Use Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Churchill Medical Systems Fluid Transfer Set General Hospital and Personal Use Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Churchill Medical Systems, Inc. A VYGON COMPANY PICC INSERTION TRAY General Hospital and Personal Use Devices Vygon Corporation 2 United States USFDA
Device Recall Churchill Medical Systems, Inc. A VYGON Company PICC INSERTION TRAY Kit General Hospital and Personal Use Devices Vygon Corporation 2 United States USFDA
Device Recall Churchill Medical Systems, Inc. A VYGON Company PICC LINE TRAY Kit General Hospital and Personal Use Devices Vygon Corporation 2 United States USFDA
Device Recall Churchill Medical Systems, Inc. DRESSING CHANGE KIT General Hospital and Personal Use Devices Vygon Corporation 2 United States USFDA
Device Recall Churchill Medical Systems, Inc. PORTACATH Tray Kit General Hospital and Personal Use Devices Vygon Corporation 2 United States USFDA
Device Recall Churchill Medical Systems, Inc. VAD ACCESS TRAY Kit General Hospital and Personal Use Devices Vygon Corporation 2 United States USFDA
Device Recall Churchill Medical Systems, Inc. VAD ACCESS TRAY Kit General Hospital and Personal Use Devices Vygon Corporation 2 United States USFDA
Device Recall Churchill Medical Systems LifeGuard General Hospital and Personal Use Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall FMI 105"Oral Surgery Administration Set General Hospital and Personal Use Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Huber Needle Set, 19Ga X 1 General Hospital and Personal Use Devices Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Lifeguard Infusion Set with Smartsite, 20Ga, 1 General Hospital and Personal Use Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Maximum Barrier Insertion Tray General Hospital and Personal Use Devices Vygon U.S.A. 2 United States USFDA
Device Recall Maximum Barrier Tray General Hospital and Personal Use Devices Vygon U.S.A. 2 United States USFDA
Device Recall Maximum Barrier Tray General Hospital and Personal Use Devices Vygon U.S.A. 2 United States USFDA
Device Recall Neonatal PICC Tray General Hospital and Personal Use Devices Vygon U.S.A. 2 United States USFDA
Device Recall Nutrisafe 2 35 mL Syringe for Safety Connection General Hospital and Personal Use Devices Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Nutrisafe 2 Syringe Gastroenterology-Urology Devices Churchill Medical Systems, Inc. 2 United States USFDA
Device Recall Nutrisafe 2 Syringe Gastroenterology-Urology Devices Churchill Medical Systems, Inc. 2 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.