Alerta De Seguridad para DELTA XTEND Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants

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

¿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
    2017-09-15
  • Fecha de publicación del evento
    2017-09-15
  • 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: depuy delta xtend reverse shoulder system modular centered and eccentric epiphysis implants medical device manufacturer, depuy, has issued a medical device safety alert concerning its delta xtend reverse shoulder system modular centered and eccentric epiphysis implants. the affected devices are identified as the following:- part description: i) modular centered epiphysis size 1 ha; ii) modular eccentric epiphysis size 1 left ha part numbers: i) 130720101; ii) 130720102 lot numbers: i) 5281492 and 5276801; ii) 5289608 and 5280184 the manufacturer’s investigation determined that the affected lots produced in a specific machine were manufactured in a manner in which the post’s diameter is out-of-specification. further investigation determined that the issue is related to the circularity of the cylinder. the circularity issue may cause the epiphysis to interfere with the stem and the two implants (epiphysis and stem) may not be able to be assembled. according to the manufacturer, there are two potential instances in which the patient could be affected: if the epiphysis does not assemble to the stem and an alternative device is available, there may be a surgical delay of 15 to 59 minutes. if the epiphysis does not assemble to the stem and there is not an alternative implant available, the patient’s wound may need to be closed and the patient scheduled for a reoperation when a suitable device is available. according to the local supplier, the affected products are not distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 15 september 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: DePuy DELTA XTEND Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants
  • Manufacturer

Manufacturer