Alerte Ou Avis De Sécurité sur ADVIA Centaur and ADVIA Centaur XP

Selon Medicines and Healthcare products Regulatory Agency, ce/cet/cette alerte ou avis de sécurité concerne un dispositif en/au/aux/à United Kingdom qui a été fabriqué par Siemens Healthcare Diagnostics Inc.

Qu'est-ce que c'est?

Les avis de sécurité sont des communications que les fabricants de dispositifs médicaux ou leurs représentants font parvenir en particulier aux travailleurs du secteur médical, mais aussi aux utilisateurs de ces dispositifs. Les avis de sécurité concernent les actions entreprises quant aux dispositifs présents sur le marché et peuvent inclure des rappels et des alertes.

En savoir plus sur les données ici
  • Type d'événement
    Safety alert / Field Safety Notice
  • ID de l'événement
    MDA/2013/005
  • Numéro de l'événement
    CON236897
  • Date
    2013-02-14
  • Date de publication de l'événement
    2013-02-14
  • Pays de l'événement
  • Source de l'événement
    MHRA
  • URL de la source de l'événement
  • Notes / Alertes
    Data from the United Kingdom is current through April 2019. All of the data comes from the Medicines and Healthcare products Regulatory Agency, 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 the United Kingdom.
  • Notes supplémentaires dans les données
  • Cause
    A failure of the wash interconnect circuit board on the advia centaur and advia centaur xp analysers may produce the following errors: 1. failure to detect that the ‘wash 1’ bottle is empty. this could result in credible but erroneous results reported on a number of tests. see affected assays listed below. or 2. incorrect indication that the ‘wash 1’ bottle is empty when actually full, causing the system to stop processing samples. siemens is planning software and hardware updates to resolve these issues by the end of march 2013. the table below summarises the assays affected and what the potential effect is for each. assay type assay potential effect on assay results auto-immune ana false positive or negative bone vitd false positive or negative cardiovascular bnp, high bias ddimer, false positive or negative tniultra always elevated torch and special id rubg2, false positive or negative rubm, false positive or negative toxg, false positive toxm false positive reproductive endocrinology dheas, false positive or negative ee2, false positive or negative shbg false positive or negative infectious disease ahavm, false positive ahavt/havt, low bias ahbcm, false negative ahbct/hbct, false negative ahbe, high or low bias ahbs, false positive ahbs, false positive ahbs2, false positive or negative ahcv, false positive or negative chiv, false positive or negative cmvg, false positive or negative conf, false positive or negative ehiv, false positive hbeag, false positive hbs, false positive hiv, false positive or negative pct, false positive or negative syph false positive or negative immunosuppressant csa low bias liver fibrosis ha,  false positive or negative piinp, false positive or negative timp1 false positive or negative tumour markers / oncology ca153, false positive ca19-9, false positive ca199a, false positive or negative freepsa false positive or negative thyroid tsh3ul false positive or negative.
  • Action
    Identify if you have affected devices. Follow the manufacturer’s recommendations in the FSN to: Monitor ‘Wash 1’ fluid levels manually. Replace the ‘Wash 1’ bottle before the fluid is depleted. Clear incorrect status or error messages that prohibit testing. Contrary to the manufacturer’s FSN, consider the need to review previous results.

Device

  • Modèle / numéro de série
  • Description du dispositif
    Laboratory analysers for a variety of tests including HIV, tumour markers and hepatitis. Specific assays. Laboratory analysers: ADVIA Centaur ® and ADVIA Centaur ® XP. Specific catalogue numbers. The following assay systems are affected by this alert: ADVIA Centaur system (Cat. 078-A001-xx) ADVIA Centaur refurbished (Cat. 078-A002R02) ADVIA Centaur XP system (Cat. 078-A011-03) ADVIA Centaur XP refurbished (Cat 078-A011R03)
  • Manufacturer

Manufacturer

  • Société-mère du fabricant (2017)
  • Source
    MHRA