Alerta De Seguridad para T-PAL, Technique Guide

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

¿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
    2014-08-01
  • Fecha de publicación del evento
    2014-08-01
  • 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: synthes t-pal, technique guide medical device manufacturer, synthes gmbh, has issued a medical device labeling update concerning its t-pal, technique guide [part no.: 036.001.088; updated revision ad; outdated revisions: aa, ab, ac]. the manufacturer updated the t-pal technique guide (pn 036.001.088) on page 19, 21 and 47 to clarify instrument handling of the t-pal applicator (pn 03.812.001 applicator outer shaft, pn 03.812.004 applicator knob). faulty handling of the t-pal applicator instrument potentially contributes to failure of the applicator inner shaft (pn 03.812.003) during insertion of implants or the non-detachable t-pal trial implants (pn 03.812.307-317 and 03.812.507-517). according to the manufacturer, if the inner shaft should break, the trial (or implant) spacer will no longer be secured in the 0o position. this rigid position is necessary for insertion; in the pivoting position, the assembly cannot be properly advanced into the disc space. furthermore, loss of rigidity during advancement of the trial (implant) into disc space could result in loss of tactile control by the surgeon. this failure is known to have resulted in a significant surgery delay and minor vascular injury. depending upon the stage of surgery, if the failure were to occur the potential harms in a worst case scenario could be: serious surgical delay; injuries to the spinal cord or cauda equina, meninges, and/or spinal nerve; damage to soft tissue; vascular damage. the manufacturer has not had any complaints of the above-mentioned events to date. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 01 aug 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Synthes T-PAL, Technique Guide
  • Manufacturer

Manufacturer