Device Recall Siemens ADVIA Centaur MultiDiluent 1

  • Modèle / numéro de série
    Lot # Expiry Date 2 Pack 76129 22 JUN 2012  77542 22 JUN 2012  78696 22 JUN 2012  80828 26 SEP 2012  80857 26 SEP 2012  81441 26 SEP 2012  82189 26 SEP 2012  83647 26 SEP 2012  84772 26 SEP 2012  86037 13 JAN 2013  86783 13 JAN 2013  88712 13 JAN 2013  90056 13 JAN 2013  91002 13 JAN 2013  93126 13 JAN 2013  6 Pack 76102 22 JUN 2012  76432 22 JUN 2012  77075 22 JUN 2012  78264 22 JUN 2012  79037 22 JUN 2012  81006 26 SEP 2012  82539 26 SEP 2012  83321 26 SEP 2012  84123 26 SEP 2012  85795 13 JAN 2013  86698 13 JAN 2013  88318 13 JAN 2013  89286 13 JAN 2013  90490 13 JAN 2013  91672 13 JAN 2013  93129 13 JAN 2013
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution-USA (nationwide) and the countries of Canada, Argentina, Australia, Brazil, Chile, China, Croatia, Denmark, Ecuduar, Egypt,Guatemala, Hong Kong,India,Ireland, Israel,India, Japan,Korea, Mexico, Malyasia, Peru, Pakistan, Saudi Arabia,Singapore, Thailand,Uruguay, Viet Nam, and South Africa.
  • Description du dispositif
    Siemens ADVIA Centaur Multi-Diluent 1 - Used for automated dilutions for the ADVIA Centaur BNP and TSH3 Ultra assays when on-board the ADVIA Centaur or ADVIA Centaur XP systems. || Catalog Numbers: || 2 Pack REF 07907174 (110312) || 6 Pack REF 07293184 (110313). || Used for automated dilutions for the ADVIA Centaur BNP and TSH3 Ultra assays when on-board the ADVIA Centaur or ADVIA Centaur XP systems.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Siemens Healthcare Diagnostics, Inc, 333 Coney St, East Walpole MA 02032-1516
  • Société-mère du fabricant (2017)
  • Source
    USFDA