Retiro De Equipo (Recall) de iChemVELOCITY Automated Urine Chemistry Systems equipped with Colour/Clarity/Specific Gravity Module. 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 Beckman Coulter Australia Pty Ltd.

¿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-2017-RN-00477-1
  • Clase de Riesgo del Evento
    Class III
  • Fecha de inicio del evento
    2017-04-20
  • País del evento
  • Fuente del evento
    DHTGA
  • URL de la fuente del evento
  • 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
    The ichemvelocity colour/clarity/specific gravity module (cgm) detects and reports 11 colours as opposed to the 18 listed in the ichemvelocity operator’s manual. if the ichemvelocity automated urine chemistry system is equipped with any of the affected cgm part numbers, the following urine colours will be detected and correctly reported: colourless, straw, light yellow, yellow, dark yellow, light amber, amber, dark amber, red, blue, and green. the following urine colours will not be detected or reported: orange, light brown, brown, dark brown, light red, dark red, other. there may be a discordance between the colour of the urine that is visually apparent and the colour that is reported, for the affected colours. in a worst case scenario, a discordant urine colour might prompt an additional non-invasive workup such as a repeat urinalysis or further testing. the results from the urine chemistry and microscopy will still be correctly reported.
  • Acción
    Beckman Coulter is advising users that the iChemVELOCITY Operator’s Manual will be updated to reflect colours that can be detected and reported by the affected CGMs. Furthermore, if the urine colour orange, light brown, brown, dark brown, light red, dark red or other colour than those listed as ‘can be detected and reported’ is visually observed during processing, it is recommended that users: - Consider reporting the visually observed colour reading using the laboratory’s reporting system (e.g. hardcopy, LIS). - Consider using an approved back-up analyser to process and report these samples if the colours above are needed within the laboratory.

Device

  • Modelo / Serial
    iChemVELOCITY Automated Urine Chemistry Systems equipped with Colour/Clarity/Specific Gravity Module. An in vitro diagnostic medical device (IVD)System Reference Numbers: 800-3564, 800-7100, 800-7103, 800-7162, 800-7163, 800-7166, 800-3061Colour/Clarity/Specific Gravity Module Reference Numbers; 700-7602, 700-7611, B93997ARTG Number: 181116
  • Manufacturer

Manufacturer