Device Recall Siemens LANTIS System ; LANTIS Commander, 10 Users ; LANTIS 6.1 Commander ; LANTIS 8.3 Commander

  • Model / Serial
    Material nos.: 4503178, 5493072, and 8148178 with serial nos.: 93-0695 93-0693 93-0938 93-1010 93-0730 93-0454 93-0759 93-0848 93-0884 93-1158 93-0584 93-0037 93-1053 93-0726 93-0588 93-0614 93-0566 93-1038 93-0648 93-0803 93-0813 93-1387 93-0278 93-0856 93-0314 93-0657 93-0222 93-1438 93-0662 93-0779 93-0732 93-0841 93-1045 93-0487 93-0564 93-0577 93-0792 93-0231 93-0096 93-0846 93-0574 93-0668 93-0634 93-0887 93-1145 93-0818 93-0102 93-0764 93-0501 93-0490 93-0261 93-0570 93-0739 93-1133 93-0159 93-0872 93-1531 93-0660 93-0798 93-0528 93-0326 93-0393 93-0738 93-0545 93-1296 93-0623 93-0370 93-1381 93-0951 93-0667 93-1135 93-0141 93-0786 93-0483 93-0385 93-0694 93-0883 93-1314 93-1320 93-0799 93-0456 93-0416 93-0838 93-0639 93-0659 93-0760 93-0608 93-0766 93-0912 93-0063 93-0262 93-0878 93-0861 93-0452 93-0533 93-0272 93-0724 93-0596 93-0831 93-0398 93-0805 93-0870 93-0874 93-0789 93-0686 93-0475 93-0748 93-1185
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution
  • Product Description
    Siemens LANTIS System ; LANTIS Commander, 10 Users ; LANTIS 6.1 Commander ; LANTIS 8.3 Commander || The intended use of the linear accelerator is to deliver x-ray radiation for therapeutic treatment of cancer.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Siemens Medical Solutions USA, Inc, 51 Valley Stream Pkwy, Malvern PA 19355
  • Manufacturer Parent Company (2017)
  • Source
    USFDA