Device Recall iSert Intraocular Lens (Model PC60AD)

  • Modèle / numéro de série
    This recall pertains to all serial numbers of I-ISO Model FC-60AD & PC-60AD lenses shipped to the U.S. and affected by this recall. A list of all affected serial numbers will be provided to the FDA LA District office. The total number of products on recall are 7355 different serial numbers on a excel spread sheet that will be attached when the Recall recommendation is sent to CDRH.
  • Classification du dispositif
  • Classe de dispositif
    3
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution
  • Description du dispositif
    iSert Intraocular Lens (Model PC-60AD)
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Hoya Surgical Optics, Inc., 14768 Pipeline Ave, Chino Hills CA 91709-3594
  • Société-mère du fabricant (2017)
  • Source
    USFDA