Alerta De Seguridad para Reduction Instrument for Spondylolisthesis, standard, for Matrix 5.5

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
    2013-06-18
  • Fecha de publicación del evento
    2013-06-18
  • 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 reduction instrument for spondylolisthesis, standard, for matrix 5.5 medical device manufacturer, synthes issued a medical device safety alert concerning reduction instrument for spondylolisthesis, standard, for matrix 5.5 (part number: 03.632.008; lot numbers: all). synthes received complaints that during spine surgery using the reduction instrument for spondylolisthesis, standard, for matrix 5.5 (03.632.008), the reduction insert broke and pieces broke off. once the reduction insert breaks, the instrument does not function as required. synthes explained that in a hypothetical worst case scenario, if the insert breaks and fragment(s) are retained, they may not be retrieved. additional operative time may be required to attempt retrieval and x-ray may not be effective to confirm that all fragments have been retrieved because the fragments are radiolucent. if fragments are retained there is a potential for an unfavorable response to the foreign material (chemical, biological or physical) within the body (including implant-related metal debris, wear particles, non-biocompatible materials) to occur which may trigger a localised reaction. the patient may be symptomatic requiring treatment and non-surgical treatment will not be effective as the disease progresses requiring revision surgery or reoperation. if treated on time, no permanent impairment is expected. according to the manufacturer, misassembly of the instrument in the operating room is a probable root cause of this safety issue. synthes has decided to remove the product from the market. according to the local supplier, the affected products were not distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 18 jun 2013.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Synthes Reduction Instrument for Spondylolisthesis, standard, for Matrix 5.5
  • Manufacturer

Manufacturer