Alerte De Sécurité sur VITROS * FOR PHENITOIN PHYT Technical Name: PHENYTOIN ANVISA Registration Number: 10132590219 Hazard Class: II Affected Model: VITROS * DRY REACTIVE FOR PHYTENIN PHENITOIN 5 cartridges with 18 slides VITROS Chemistry Products PHYT Slides , product code 8298671, lots: 1401566241, 1401566904, 1401577639, 1401578552, 1401578552, 1401580410, 1401589627, 1401591230, 1401592935, 1401604105 and 1401614738. The Assay Data Diskette (ADD) and Calibration 16607 products are not applicable.

Selon Agência Nacional de Vigilância Sanitária (ANVISA), ce/cet/cette alerte de sécurité concerne un dispositif en/au/aux/à Brazil qui a été fabriqué par Johnson & Johnson do Brasil Ind. e Com. de Prod. para Saúde Ltda; Ortho-Clinical Diagnostics, Inc..

Qu'est-ce que c'est?

Les alertes fournissent des informations importantes et des recommandations concernant les dispositifs médicaux. Le fait qu'une alerte soit émise ne signifie pas nécessairement qu'un dispositif soit dangereux. Les alertes de sécurité, qui sont envoyées tant aux travailleurs du secteur médical qu'aux utilisateurs de ces dispositifs, peuvent inclure des rappels. Elles peuvent être rédigées par des fabricants mais aussi par des autorités en charge de la santé.

En savoir plus sur les données ici
  • Type d'événement
    Safety alert
  • ID de l'événement
    2107
  • Date
    2016-12-18
  • Pays de l'événement
  • Source de l'événement
    ANVISA
  • URL de la source de l'événement
  • Notes / Alertes
    Brazilian data is current through June 2018. All of the data comes from Anvisa, 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 Brazil.
  • Notes supplémentaires dans les données
    Some instructions are recommended: 1) Install the Calibration Diskette / ADD DRV 5910 or later diskette in the system: The automatic download will be available for the e-Connected systems as of December 2, 2016; The Calibration Diskette and / or ADD diskette will also be sent to your installation upon availability. IMPORTANT NOTE: After charging the DRV 5910 (or later) for the first time, VITROS PHYT Slides will lose calibration and recalibrate. In the meantime, it is acceptable to continue using the product. 2) After successful calibration and quality control evaluation, it is acceptable to use existing inventory of VITROS PHYT Slides. 3) Place this notification on the VITROS System or along with the user documentation. 4) Fill out and return the Receipt Confirmation Form.
  • Cause
    This notice provides additional information from a product correction notification that ortho clinical diagnostics (ortho) issued in december 2015 regarding clarification of the operator's actions for laundering errors. since then, the occurrence of u90-382 or 6lu condition codes associated with wash errors has been monitored and an increase in wash errors has been observed for vitros chemistry products phyt slides.
  • Action
    Field Action Code 16000169 triggered under the responsibility of Johnson & Johnson do Brasil Ind. And Com. De Prod. for Health Ltda. Company will make correction in the field.