Alerta De Seguridad para Corporation Citrate Activated Partial Thromboplastin Time (APTT) Cuvettes

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

¿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
    2014-01-03
  • Fecha de publicación del evento
    2014-01-03
  • 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: international technidyne corporation citrate activated partial thromboplastin time (aptt) cuvettes the australia therapeutic goods administration (tga) posted a medical device safety alert concerning citrate activated partial thromboplastin time (aptt) cuvettes manufactured by international technidyne corporation.The affected lot numbers are e3jcc013-p1 and e3jcc014-p2 and the expiration date is may 2014. the manufacturer has determined that citrate aptt cuvettes from the lots listed above may recover higher than expected results in normal individuals. the manufacturer's investigation into the affected lots identified that when performing tests on non-heparinized e.G., normal blood samples, results may average higher than historic values. test results performed on patients receiving heparin therapy are not affected. the manufacturer has evaluated the risk to health using the affected device and has determined under a variety of clinical conditions, an erroneous increase in the citrated aptt baseline may contribute to serious injury. customers are requested to inspect their stock and quarantine all affected lots of the product, which will be arranged for recovery and replacement. customers are also advised to discuss with the laboratory director about the requirement for retesting of reported patient results. for details, please visit the following tga website: http://www.Tga.Gov.Au/sara/arn-detail.Aspx?k=rc-2013-rn-01364-1 if you are in possession of the affected product, please contact your supplier for necessary actions. posted on 3 january 2014.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: International Technidyne Corporation Citrate Activated Partial Thromboplastin Time (APTT) Cuvettes
  • Manufacturer

Manufacturer