Alerta De Seguridad para ABGII Modular Femoral Stem and Modular Neck

Según Department of Health, este evento ( alerta de seguridad ) involucró a un dispositivo médico en Hong Kong que fue producido por Stryker Australia Pty Ltd.

¿Qué es esto?

Las alertas proporcionan información importante y recomendaciones sobre los productos. Aunque se haya emitido una alerta, esto no significa necesariamente que el producto se considera peligroso. Las alertas de seguridad, dirigidas a trabajadores de la salud y a usuarios, pueden incluir retiro de equipos. Pueden ser escritas por los fabricantes, pero también por funcionarios del área de salud.

Más información acerca de la data acá
  • Tipo de evento
    Safety alert
  • Fecha
    2012-07-23
  • Fecha de publicación del evento
    2012-07-23
  • País del evento
  • Fuente del evento
    DH
  • URL de la fuente del evento
  • Notas / Alertas
    Hong Kong data is current through September 2018. All of the data comes from the Department of Health (Hong Kong), except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Hong Kong.
  • Notas adicionales en la data
    Medical Device Safety Alert
  • Causa
    Medical device safety alert: stryker australia pty ltd abgii modular femoral stem and modular neck the therapeutic goods administration (tga), australia issued a medical device safety alert concerning abgii modular femoral stem and modular neck manufactured by stryker australia pty ltd. according to the manufacturer, there is potential for fretting and corrosion at the join between the femoral stem and the neck component of the abgii modular system. fretting and corrosion can result in metal debris in and around the hip joint. if this occurs, patients may experience inflammation, adverse local tissue reactions (altrs), hypersensitivity/allergic reactions and osteolysis (bone loss). stryker australia pty ltd has contacted every australian orthopaedic surgeon who has ever implanted the abgii modular hip replacement system. those surgeons have been asked to contact their patients to discuss what clinical action is most appropriate. if the results reveal that adverse local tissue reaction of patients are due to metal wear debris, the surgeon should consider proceeding with a revision of the femoral component to a monolithic stem. the manufacturer also advised patients that if experiencing hip or thigh pain, or are concerned about the hip replacement, they should contact their implanting surgeon to arrange a review appointment. for details, please refer to tga website http://www.Tga.Gov.Au/safety/alerts-device-abgii-120720.Htm. posted on 23 july 2012.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Stryker Australia Pty Ltd ABGII Modular Femoral Stem and Modular Neck
  • Manufacturer

Manufacturer

  • Empresa matriz del fabricante (2017)
  • Source
    DH