Alerta De Seguridad para Mandible Distractor, Monoaxial and Proximal Foot Plate

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

¿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
    2016-06-15
  • Fecha de publicación del evento
    2016-06-15
  • 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: mandible distractor, monoaxial and proximal foot plate medical device manufacturer, synthes, has issued a medical device safety alert concerning its mandible distractor, monoaxial and proximal foot plate. according to the manufacturer, the fastener on the mandible distractor may become prematurely separated from the proximal foot plate. in the event that the mandible distractor becomes disengaged from the proximal foot plate during device implantation, surgical delay may occur if another device is not available in the surgical suite. if the mandible distractor becomes disengaged from the proximal foot plate after device implantation, repeat surgery may be required to replace the mandible distractor/foot plates. there may be a risk of local infection as a result of repeat surgery caused by the disengagement since the product is in the oral cavity. there is no replacement device available from the manufacturer. the manufacturer offers several alternative devices which are also intended for distraction of the mandible, including the stainless steel mandible distractor system, the titanium multi-vector distractor module system, and the curvilinear distraction system. according to the local supplier, the following affected products are distributed in hong kong:-. a) mandible distractor, monoaxial, left, distraction length 30mm [part number: 487.965, lot number: 6538904] b) proximal foot plate, left, f/mandib. distractor, monoaxial [part number: 487.975, lot number: 7865426] if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 15 june 2016.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Mandible Distractor, Monoaxial and Proximal Foot Plate
  • Manufacturer

Manufacturer