Device Recall ABL 800 FLEX analyzers

  • Modèle / numéro de série
    ABL 800 FLEX series blood gas analyzers containing software version 5.24.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    The recalled analyzers were distributed to customers nationwide throughout the U.S. and in some parts of Canada.
  • Description du dispositif
    ABL 800 FLEX series blood gas analyzers containing software version 5.24.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Radiometer America Inc, 810 Sharon Dr, Westlake OH 44145-1598
  • Source
    USFDA