Alerta De Seguridad para Midface Distractor, complete, distraction length 40 mm, Titanium Alloy (TAN)

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
    2014-01-22
  • Fecha de publicación del evento
    2014-01-22
  • 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 gmbh midface distractor, complete, distraction length 40 mm, titanium alloy (tan) medical device manufacturer, synthes gmbh, has issued a field safety notice concerning midface distractor, complete, distraction length 40 mm, titanium alloy (tan) (part number: 487.982; lot number: prior to 6913910). as the tab of some distractors may be oversized, there is the potential for the anterior footplates not to fit onto the midface distractor assembly (part number 487.982). because recognition of the defined defect may not be detected until the intraoperative patient treatment period, there is the potential that the index surgical goals will not be achieved and a second unanticipated surgical intervention would be required. according to the manufacturer, there have been no adverse events associated with this issue. the manufacturer advises users to quarantine and return all unused affected products. according to the local supplier, the affected products were distributed in hong kong. if you are in possession of the products, please contact your supplier for necessary actions. posted on 22 january 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Synthes GmbH Midface Distractor, complete, distraction length 40 mm, Titanium Alloy (TAN)
  • Manufacturer

Manufacturer