Device Recall Guidant RAPIDO CutAway Guiding Catheter

  • Modèle / numéro de série
    Lot Number: 0120891 and 0121091
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide distribution, and Ireland.
  • Description du dispositif
    Guidant RAPIDO Cut-Away Guiding Catheter, 6F. || Part Numbers: 66676-201 and 667552-100. || For use in cardiac diagnostic and therapeutic procedures.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Abbott Vascular, 26531 Ynez Rd, Temecula CA 92591-4630
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    USFDA