{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Palo Alto",
      "address_1": "911 Hansen Way",
      "reason_for_recall": "Some X-jaw (lower collimator jaw) carriers were made using the incorrect metal alloy, which can cause the jaw carrier to crack. If both carriers on the same X-jaw crack, the jaw would be able to move freely in the closed direction.  The position readout interlock circuitry will not detect this jaw position deviation. This may lead to treatment with an under-dose of the intended target volume.",
      "address_2": "",
      "product_quantity": "221 Units",
      "code_info": "LIST OF SERIAL NUMBERS:    H140863 ,H294608 ,H294669 ,H294732  ,H140865 ,H294610 ,H294670 ,H294733  ,H140866 ,H294611 ,H294671 ,H294734  ,H140867 ,H294612 ,H294672 ,H294735  ,H140868 ,H294613 ,H294673 ,H294736  ,H140869 ,H294614 ,H294674 ,H294737  ,H140870 ,H294615 ,H294675 ,H294738  ,H140871 ,H294616 ,H294676 ,H294739  ,H140872 ,H294617 ,H294677 ,H294740  ,H140873 ,H294618 ,H294678 ,H294741  ,H140874 ,H294619 ,H294679 ,H294742  ,H140875 ,H294620 ,H294680 ,H294743  ,H140876 ,H294621 ,H294681 ,H294744  ,H140877 ,H294622 ,H294682 ,H294745  ,H140878 ,H294623 ,H294683 ,H294746  ,H140879 ,H294624 ,H294684 ,H294747  ,H140880 ,H294625 ,H294685 ,H294748  ,H140881 ,H294626 ,H294686 ,H294749  ,H140882 ,H294627 ,H294687 ,H294750  ,H140883 ,H294628 ,H294688 ,H294751  ,H140884 ,H294629 ,H294689 ,H294752  ,H140885 ,H294630 ,H294690 ,H294753  ,H140886 ,H294631 ,H294691 ,H294754  ,H140887 ,H294632 ,H294692 ,H294755  ,H140888 ,H294633 ,H294693 ,H294756  ,H140889 ,H294634 ,H294694 ,H294757  ,H140890 ,H294635 ,H294695 ,H294758  ,H140891 ,H294636 ,H294696 ,H294759  ,H140892 ,H294637 ,H294697 ,H294760  ,H140893 ,H294638 ,H294698 ,H294761  ,H140895 ,H294639 ,H294699 ,H294762  ,H140896 ,H294640 ,H294700 ,H294763  ,H140897 ,H294641 ,H294701 ,H294764  ,H140898 ,H294642 ,H294702 ,H294765  ,H140899 ,H294643 ,H294704 ,H294766  ,H140900 ,H294644 ,H294705 ,H294767  ,H181175 ,H294645 ,H294706 ,H294768  ,H181176 ,H294646 ,H294707 ,H294769  ,H181177 ,H294647 ,H294708 ,H294770  ,H181178 ,H294648 ,H294709 ,H294771  ,H181179 ,H294649 ,H294710 ,H294772  ,H181180 ,H294650 ,H294711   ,H181181 ,H294651 ,H294712   ,H181182 ,H294652 ,H294713   ,H181183 ,H294653 ,H294714   ,H181184 ,H294654 ,H294715   ,H181185 ,H294655 ,H294716   ,H181186 ,H294656 ,H294717   ,H181187 ,H294657 ,H294718   ,H181188 ,H294658 ,H294719   ,H181189 ,H294659 ,H294720   ,H181190 ,H294660 ,H294722   ,H181191 ,H294661 ,H294723   ,H181192 ,H294662 ,H294724   ,H182000 ,H294663 ,H294726   ,H182001 ,H294664 ,H294727   ,H182002 ,H294665 ,H294728   ,H182003 ,H294666 ,H294729   ,H182005 ,H294667 ,H294730   ,H294607 ,H294668 ,H294731",
      "center_classification_date": "20120914",
      "distribution_pattern": "Worldwide Distribution.",
      "state": "CA",
      "product_description": "Varian brand Clinac, Trilogy, Novalis Tx, Unique, linear accelerators; Model Number: H14, H18, H29,  Reference/FSCA Identifier: CP-08881; Product is manufactured and distributed by Varian Medical Systems Inc., Palo Alto, CA.    1) The Varian Low Energy Linear Accelerator is indicated for precision radiotherapy for lesions, tumors and conditions anywhere in the body when radiation treatment i is indicated. (2) The Varian High Energy Linear Accelerator is indicated for stereotactic radiosurgery and precision radiotherapy for lesions, tumors and conditions anywhere in the body when radiation treatment is indicated.",
      "report_date": "20120926",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Varian Medical Systems, Inc. Oncology Systems",
      "recall_number": "Z-2383-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63033",
      "termination_date": "20131204",
      "more_code_info": "",
      "recall_initiation_date": "20120814",
      "postal_code": "94304-1028",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}