Device Recall Heartstring II Proximal Seal aortic cutter

  • Modèle / numéro de série
    HSK-2038, HSK-2043. All lots are affected by this recall.
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Product was distributed to 274 consignees. 15 are international distributors. 259 hospitals. The product is fully distributed to the following countries: USA, Belgium, CAnada, Czech Republic, Denmark, Finland, France, Germany, Great Britain, Greece, Israel, Italy, Lebanon, Netherlands, Poland, Portugal, Slovakia, Slovenia, Spain, and Swizerland. 3 VAs received product: 13000 Bruce B Downs Blvd, Tampla, FL, 800 Hospital Dr., columbia, MO, and 921 NE 13th st., Oklahoma City, OK.
  • Description du dispositif
    Aortic Cutter, single use device consisting of grip, cutter, aortic stops, needle, safety lock and actuation button.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Guidant Cardiac Surgery, 3200 Lakeside Dr, Santa Clara CA 95054-2807
  • Source
    USFDA