Alerta De Seguridad para DxH 500 Hematology Analyser

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

¿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
    2017-05-29
  • Fecha de publicación del evento
    2017-05-29
  • 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: beckman coulter dxh 500 hematology analyser medical device manufacturer, beckman coulter, has issued a medical device safety alert concerning its dxh 500 hematology analyser [reference: b40601; software versions 1.0.2]. as a result of internal investigations, the manufacturer has become aware that when the instrument temperature (<18°c to >36.5°c) is exceeded, the dxh 500 allows sample processing and result reporting despite the instructions for use stating that “the run sample is inaccessible”. results generated in this scenario may be erroneous. additionally: the message on the results screen/printout reads “instrument temperature” instead of “instrument temperature out of range”. the results are transmitted to the laboratory information system (lis) without the accompanying “instrument temperature out of range” message. using the auto-transmit option could lead to the release of erroneous results to the lis. if the instrument is operating out of the temperature range and the warnings on the screen are ignored and the results are used, then: these cbc, wbc-diff or cbc/wbc-diff results may be erroneous. if these erroneous results are released to the physician, this could result in inappropriate patient management. the manufacturer advises affected users to take the following actions:- when the message “instrument temperature out of range” or “instrument temperature” is displayed on the system or printouts, do not report the patient results. ensure the laboratory ambient temperature is within specifications (18°c -32°c) when processing samples. disable the auto-transmit option if there is a potential for the operational temperature to be exceeded. consult with the medical director to determine if a retrospective review of results is warranted. this issue will be corrected in a future software release. 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 29 may 2017.

Device

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Beckman Coulter DxH 500 Hematology Analyser
  • Manufacturer

Manufacturer