Device Recall Theratron 780E

  • Model / Serial
    Model Theratron 780E
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    The products were shipped to medical facilities in FL and KS. The product was also shipped to Kuwait, Spain, Honduras, Romania, France, Grrece, Bangladesh, Germany, Nepal, Canada, England, Thailand, Phillippines, Mexico, Columbia, India, Switzerland, Syria, Trinidad & Tobago, Ireland, Turkey, Algeria, Portugal, Poland, Iran, China, Cuba, Belgium, Hungary, Egypt, Italy, Vietnam, Sri Lanka, and Costa Rica.
  • Product Description
    Theratron 780E Cobalt Radiotherapy
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    MDS Canada Inc. DBA MDS Nordion, 447 March Road, Kanata Canada
  • Source
    USFDA