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  • Dispositivo 298
  • Fabricante 1
  • Evento 124969
  • Implante 0
Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall Breast Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Breast Augmentation Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Bleph Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Bayview Breast Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Bayview Abdominoplasty Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Basin Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Basic Tray General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Basic Setup Tray General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Basic Setup Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Basic Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Basic Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Basic Kit General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Basic Face Kit General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Basic Extended Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Augmentation Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Arthroscopy Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Arthroscopy Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Anterior Cervical Fusion Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Angio Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Abdominoplasty Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall General Surgery Packs General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Laparotomy Pack Latex Free General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall Laparotomy Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 2 United States USFDA
Device Recall AMS 4675 Angio Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 1 United States USFDA
Device Recall AMS 4674 Custom Pack General and Plastic Surgery Devices Windstone Medical Packaging, Inc. 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.