Events

Alerte De Sécurité sur Name of products: Calibrator Kit 29 Vitros *, RegANVISA 80145900910. Product classified as II and the control of these systems is carried out by lot number. 89 units of the reagent kit were imported. Product code 6802344, Lots affected and imported into Brazil: 2915, 2995

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.

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
    1945
  • Date
    2016-07-12
  • Pays de l'événement
    Brazil
  • Source de l'événement
    ANVISA
  • URL de la source de l'événement
    http://www.anvisa.gov.br/sistec/alerta/consultaralerta.asp
  • 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
    If you have any questions regarding this field action, please contact Johnson & Johnson do Brasil Ind. And Com. De Prod. for Health Ltda. by telephone: 12 3932-7977 or e-mail: gbuosi@its.jnj.com Recommendations to users: Action required for laboratories that have the affected lot: • As soon as available, install ADD DRV 5884 or later on your system VITROS. o Connected Systems: Automatic download will be available in early May 2016. o ADD DRV 5884 or later will also be sent to your facility upon availability. NOTE: After loading ADD DRV 5884 or later for the first time, the VITROS dTIBC GEN 30 Reagent will lose the calibration and must be recalibrated. • After successful calibration and quality control evaluation, it is acceptable to use your remaining inventory of the VITROS dTIBC, GEN 30 Reagent. • Place this notification on your VITROS System or along with your user documentation. • Complete and return the Receipt Confirmation form
  • Cause
    The manufacturer has detected that there are incorrect values ​​(data / calibration math) on assay data diskettes (add) for calibrator kit 29, which supports the vitros dtibc, gen 30 reagent. incorrect values ​​will cause a positive trend in the sample results (ie, patient samples, proficiency fluids, and quality control fluids).
  • Action
    Action code 16000095. Sending of the Letter to the Clients // Recommendations to the users.

Device

Name of products: Calibrator Kit 29 Vitros *, RegANVISA 80145900910. Product classified as II and...

Manufacturer

Johnson & Johnson do Brasil Ind. e Com. de Prod. para Saúde Ltda; ORTHO CLINICAL DIAGNOSTICS