Events

Retiro De Equipo (Recall) de m24sp Instrument System (sample extraction system). An in vitro diagnostic medical device (IVD)

Según Department of Health, Therapeutic Goods Administration, este evento ( retiro de equipo (recall) ) involucró a un dispositivo médico en Australia que fue producido por Abbott Australasia Pty Ltd Molecular Division.

¿Qué es esto?

Una corrección al equipo o acción de retiro tomada por el fabricante para abordar un problema con un dispositivo médico. Los retiros (recalls) ocurren cuando un dispositivo médico está defectuoso, cuando puede poner en riesgo la salud, o cuando simultáneamente está defectuoso y puede poner en riesgo la salud.

Más información acerca de la data acá
  • Tipo de evento
    Recall
  • ID del evento
    RC-2014-RN-01010-1
  • Clase de Riesgo del Evento
    Class II
  • Fecha de inicio del evento
    2014-09-18
  • País del evento
    Australia
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2014-RN-01010-1
  • Notas / Alertas
    Australian data is current through July 2018. All of the data comes from the Australian Therapeutic Goods Administration, 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 recall data from the U.S. and Australia.
  • Notas adicionales en la data
  • Causa
    Abbott molecular has identified that when duplicate sample ids are used for multiple replicates of a sample, calibrator or control in the same run: some samples may not be included in the plate report; some duplicate sample ids are reassigned a unique identifier by the software and a warning message is displayed in the plate report. these issues occur if duplicate sample ids are used within a run, on the m24sp plate report. the m24sp plate report is a pdf file generated by the software for each instrument run. it provides a list of sample id’s and their processing information and error status.
  • Acción
    Abbott Molecular is advising users that to ensure proper function of the Plate Report, duplicate sample IDs should not be used on the m24sp. If two or more replicates of a sample, calibrator or control are being run, a unique sample ID should be used for each of the replicates. This action has been closed-out on 15/07/2016.

Device

m24sp Instrument System (sample extraction system). An in vitro diagnostic medical device (IVD)

Manufacturer

Abbott Australasia Pty Ltd Molecular Division
  • Empresa matriz del fabricante (2017)
    Abbott Laboratories
  • Comentario del fabricante
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    DHTGA