Events

Rappel de Sysmex CA-600 series with built-in barcode reader. An in vitro diagnostic medical device (IVD)

Selon Department of Health, Therapeutic Goods Administration, ce/cet/cette rappel concerne un dispositif en/au/aux/à Australia qui a été fabriqué par Siemens Healthcare Pty Ltd.

Qu'est-ce que c'est?

Une correction ou un retrait opéré par un fabricant afin de répondre à un problème causé par un dispositif médical. Les rappels surviennent lorsqu'un dispositif médical est défectueux, lorsqu'il pourrait poser un risque pour la santé, ou les deux à la fois.

En savoir plus sur les données ici
  • Type d'événement
    Recall
  • ID de l'événement
    RC-2017-RN-00807-1
  • Classe de risque de l'événement
    Class II
  • Date de mise en oeuvre de l'événement
    2017-06-22
  • Pays de l'événement
    Australia
  • Source de l'événement
    DHTGA
  • URL de la source de l'événement
    https://apps.tga.gov.au/Prod/sara/arn-detail.aspx?k=RC-2017-RN-00807-1
  • Notes / Alertes
    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.
  • Notes supplémentaires dans les données
  • Cause
    Siemens healthcare has been advised by sysmex corporation about a phenomenon affecting the specific sysmex ca-600 series systems. under rare circumstances there is the potential that the system might fail to alert the operator about an individual sample id number assigned to multiple patient measurement results when using the built-in barcode scanner. this may lead to an incorrect diagnostic and patient treatment decision due to potential of a mismatched result for the patient.
  • Action
    Sysmex is advising that: 1. In case an error message "Barcode Scanner Driver Error" appears during a CA-600 series sampler run with built-in barcode scanner, a blockage has stopped the barcode scanner from normal operation. The scanner cannot move from home position to #1, #2, ..#10 (all) sample tube position at the sampler rack, then back to home position. 2. Remove any block or failure. 3. Before clearing the error, confirm on the instrument display if the same sample IDs exist on the measurement results. The number of samples loaded should match the number of sample ID# displayed, & should correspond to the barcoded sample IDs for each of the samples loaded in the rack. 4. If you find anything wrong on the measurement results for the patient sample ID, reset the sample ID according to the note described in "5.11 Set Sample Nos." section of IFU. 5. Do not report previous patient results & restart analysis, verify results & sample ID No. for all specimens in the rack.

Device

Sysmex CA-600 series with built-in barcode reader. An in vitro diagnostic medical device (IVD)
  • Modèle / numéro de série
    Sysmex CA-600 series with built-in barcode reader. An in vitro diagnostic medical device (IVD)Sysmex CA-620Siemens Material Number (SMN): 10712040Sysmex CA-660Siemens Material Number (SMN): 10712039ARTG Number: 179939
  • Manufacturer
    Siemens Healthcare Pty Ltd

Manufacturer

Siemens Healthcare Pty Ltd
  • Société-mère du fabricant (2017)
    Siemens AG
  • Source
    DHTGA