Device Recall Recovery G2

  • Modèle / numéro de série
    Lot numbers: GFPK3279, GFPK3280, GFPK3281 & GFPK3282
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide including USA, Australia, and Canada
  • Description du dispositif
    Recovery G2 Filter System - Jugular/Subclavian Delivery Kit, for use in the prevention of recurrent pulmonary embolism. Catalog Number RF-220J ***For Canada & Australia only***
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Bard Peripheral Vascular Inc, 1625 W 3rd St, Tempe AZ 85281-2438
  • Société-mère du fabricant (2017)
  • Source
    USFDA