Device Recall RENEWAL 3 DS HE ICD

  • Model / Serial
    508822, 508827 and 508862
  • Product Classification
  • Device Class
    3
  • Implanted device?
    Yes
  • Distribution
    CA, IL, MI, MO, OR and PA
  • Product Description
    CONTAK RENEWAL 3 DS HE, model H177 CRT-D Cardiac Resynchronization Therapy Defibrillator. Contents have been Sterilized with gaseous ethylene oxide. Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA. Provides ventricular tachyarrhythmia and cardiac resynchronization therapies.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Guidant Corporation, 4100 Hamline Ave N, Saint Paul MN 55112-5700
  • Source
    USFDA