Device Recall IVF Pasteur Pipettes

  • Modèle / numéro de série
    160306022 EXP 1/22/2010 160306046 EXP 2/15/2010 160306065 EXP 3/6/2010
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The recalled product was distributed to 2 direct accounts in IL and to 6 international distributors in United Kingdom, Greece, Australia, United Arab Emirates, the Netherlands, and Israel.
  • Description du dispositif
    IVF Pasteur Pipettes, glass, cotton plugged, length 9", in boxes of 90 consisting of 30 nylon tube packages of 3 pipettes each. Item # PP-9-90PL. Boxes are labeled in part ***Humagen Fertility Diagnostics, Inc. 2400 Hunter's Way Charlottesville, VA 22911***
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Humagen Fertility Diagnostics, Inc., 2400 Hunters Way, Charlottesville VA 22911-7930
  • Source
    USFDA