Alerta De Seguridad para Cheek Retractor, f/MatrixMANDIBLE U-shaped, Flexible

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
    2014-12-23
  • Fecha de publicación del evento
    2014-12-23
  • 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 cheek retractor, f/matrixmandible u-shaped, flexible medical device manufacturer, synthes gmbh, has issued a medical device safety alert concerning its cheek retractor, f/matrixmandible u-shaped, flexible [part number: 397.232; lot number: 6355110]. according to the manufacturer, the cheek retractor for matrixmandible u-shaped may not function as intended due to the potential for failure and/or corrosion of the internal spring which has been manufactured from an incorrect material. there is a potential for subcomponent spring breakage originating from the incorrect raw material used in the fabrication of the spring in the cheek retractor for matrixmandible u-shaped, flexible. there is a potential for harm to patients including surgical delay if the retractor does not work during a procedure and a replacement needs to be found. adverse tissue reaction and/or infection could occur if the retractor is used and corroded material from the spring falls into the wound and is not removed during irrigation. according to the local supplier, the affected products are distributed in hong kong. if you are in possession of the affected products, please contact your supplier for necessary actions. posted on 23 december 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Synthes GmbH Cheek Retractor, f/MatrixMANDIBLE U-shaped, Flexible
  • Manufacturer

Manufacturer