{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "130514",
      "product_res_number": "Z-0152-2015",
      "event_date_initiated": "2014-10-06",
      "event_date_posted": "2014-10-30",
      "recall_status": "Terminated",
      "event_date_terminated": "2021-09-15",
      "res_event_number": "69425",
      "product_code": "IWB",
      "k_numbers": [
        "K120811"
      ],
      "product_description": "Laksell Gamma Knife Perfexion",
      "code_info": "Serial No. 6052, 6144, 6088, 6122, 6158, 6005, 6028, 6097, 6153, 6064, 6081, 6103, 6120, 6143, 6145, 6213, 6215, 6076, 6070, 6136, 6002, 6090, 6131, 6063, 6160, 6077, 6018, 6031, 6040, 6105, 6121, 6013, 6026, 6038, 6050, 6089, 6042, 6055, 6058, 6071, 6080, 6087, 6091, 6096, 9098, 6106, 6108, 6109, 6116, 6118, 6125, 6132, 6133, 6142, 6148, 6149, 6161, 6162, 6175, 6181, 6183, 6198, 6205, 6206, 6163, 6169, 6033, 6041, 6046, 6068, 6113, 6019, 6067, 6110, 6104, 6043, 6044, 6062, 6085, 6086, 6101, 6111, 6123, 6126, 6157, 6177, 6178, 6024, 6069, 6094, 6007, 6075, 6182, 6065, 6159, 6199, 6003, 6017, 6027, 6039, 6112, 6146, 6194, 6004, 6006, 6008, 6009, 6010, 6011, 6012, 6014, 6015, 6016, 6020, 6021, 6022, 6023, 6025, 6029, 6030, 6032, 6034, 6035, 6036, 6037, 6045, 6047, 6048, 6053, 6054, 6056, 6057, 6060, 6061, 6066, 6072, 6073, 6074, 6078, 6079, 6082, 6083, 6084, 6092, 6093, 6095, 6099, 6100, 6102, 6107, 6114, 6115, 6117, 6119, 6124, 6127, 6128, 6129, 6130, 6134, 6135, 6139, 6141, 6150, 6151, 6165, 6167, 6171, 6172, 6173, 6176, 6179, 6180, 6184, 6185, 6191, 6192, 6200, 6203, 6207, 6211",
      "firm_fei_number": "1037831",
      "recalling_firm": "Elekta, Inc.",
      "address_1": "400 Perimeter Center Ter Ne",
      "address_2": "Ste 50",
      "city": "Atlanta",
      "state": "GA",
      "postal_code": "30346-1227",
      "additional_info_contact": "Linda Wetsel\n770-300-9725",
      "reason_for_recall": "Elekta has become aware that the latches may be locked before they have been fully turned resulting in a poorly locked frame.",
      "root_cause_description": "Device Design",
      "action": "Elekta sent an\" Important Field Safety Notice\" distributed on October 6, 2014,  to all affected customers. The letter identified the product the problem and the action needed to be taken by the customer.   \n\nThis Important Field Safety Notice describes the problem and possible work arounds for customers to follow until a permanent solution can be developed. They are:\n\n\" Always assure that the plastic lever is only operated when at a right angle with the frame adapter.\n\" Do not force the plastic lever in place if it meets significant resistance when turned.\n\" Ensure that the plastic lever is completely flush with the frame adapter and that no angulations are present.\n\nCorrective Action #2 - Elekta will check and replace as necessary affected frame adapters in the field.  This will be released at the end of October 2014, and Elekta will have six months to complete the checks and replacements for those products in the field. \n\nIf you have any questions please contact your local Elekta office, or call (770) 300-9725.",
      "product_quantity": "181",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) including the states of AK, AZ, AR, CA, CO, CT, FL, GA, HI, IL, KY, LA, MA, MI, MN, MS, MO, MT, NJ, NM, NY, NC, OH, OR, PA, RI, SC, TX, TN, UT, VA, WA and WV, and the countries of  Australia, Austria, Belgium, Brazil, Canada, China, Colombia, Czech Republic, Egypt, France, Germany, Greece, Hong Kong, India, Indonesia, Italy, Japan, Mexico, Morocco, Netherland, Norway, Poland, Portugal, Russia, Saudi Arabia, South Korea, Spain, Sweden, Switzerland, Taiwan, Turkey and United Kingdom.",
      "openfda": {
        "k_number": [
          "K051022",
          "K160440",
          "K001006",
          "K970647",
          "K871215",
          "K142219",
          "K180571",
          "K984563",
          "K000478",
          "K925133",
          "K250391",
          "K860849",
          "K983917",
          "K222047",
          "K173789",
          "K041125",
          "K190844",
          "K780948",
          "K120811",
          "K912250",
          "K973441",
          "K092083",
          "K914808",
          "K151159",
          "K151561",
          "K203250",
          "K894165",
          "K053485",
          "K061540",
          "K200050",
          "K150191",
          "K102533",
          "K924849",
          "K061941",
          "K133565",
          "K203146",
          "K232854",
          "K063512",
          "K131777",
          "K173791",
          "K172706",
          "K984328",
          "K850543",
          "K863180",
          "K827583",
          "K964606",
          "K060314",
          "K960892"
        ],
        "registration_number": [
          "3015232217",
          "3015621321",
          "3014273653",
          "1038814",
          "9617016",
          "3006946288",
          "2939248",
          "3020999824",
          "3005136058",
          "3015620182"
        ],
        "fei_number": [
          "3015232217",
          "3002806900",
          "3015621321",
          "3014273653",
          "1038814",
          "3006946288",
          "2939248",
          "3020999824",
          "3005136058",
          "3015620182"
        ],
        "device_name": "System, Radiation Therapy, Radionuclide",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.5750",
        "device_class": "2"
      }
    }
  ]
}