{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "37987",
      "product_res_number": "Z-0817-05",
      "event_date_initiated": "2005-04-08",
      "event_date_posted": "2005-05-11",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-12-19",
      "res_event_number": "31494",
      "product_code": "IXJ",
      "k_numbers": [
        "K925997"
      ],
      "product_description": "KODAK GP FLEXIBLE PHOSPHOR SCREENS, for use with Kodak DirectView CR 500 systems.  Responsible firm on label:  Made in U.S.A. by Eastman Kodak Company, Rochester, N.Y.  14650.  Screens are sold in the following sizes and Cat. Nos:  \n\n(1) Cat. #812-7334 - 15 x 30 cm;\n(2) Cat #825-9269 - 18 x 24 cm;\n(3) Cat #167-8663 - 24 x 30 cm;\n(4) Cat #810-7823 - 35 x 35 cm;\n(5) Cat #160-5906 - 35 x 43 cm",
      "code_info": "Each screen has a 17-digit code.  Product subject to recall includes  ALL codes containing ''CE'' and ''CR'' and codes with ''CO''  with date code of ''051'' or lower. NOTE:  The date codes are the 8th thru 10th digit and equal the julian date.  The YEAR CODES are the 11th and 12th digit.   The codes are located at the top edge of the CR screen.  i.e. xxxxxxx051CO#xxxx.",
      "firm_fei_number": "1315356",
      "recalling_firm": "Eastman Kodak Co",
      "address_1": "343 State St",
      "city": "Rochester",
      "state": "NY",
      "postal_code": "14650",
      "additional_info_contact": "John P. Labella\n585-724-6891",
      "reason_for_recall": "Screens may be affected with image artifacts",
      "root_cause_description": "Other",
      "action": "Letters mailed 4/8/2005.   Customers informed of the problem and advised that Kodak representatives will exchange the recalled screens for new screens.",
      "product_quantity": "Approximately 6,900 screens",
      "distribution_pattern": "There are 263 U.S. customers; 22 Canadian customers; 74 Japanese customers;  213 Greater Asian Region customers; 19 Latin American customers; 306 Europe/Africa/ Middle East customers.",
      "openfda": {
        "k_number": [
          "K941626",
          "K964025",
          "K963893",
          "K926261",
          "K883527",
          "K945697",
          "K954294",
          "K945327",
          "K901012",
          "K854459",
          "K940309",
          "K837776",
          "K925997",
          "K926445",
          "K962338"
        ],
        "registration_number": [
          "2431224",
          "3000126629",
          "8030318",
          "1225677",
          "3002808157",
          "3003768251",
          "1450835",
          "3008141750",
          "3016674288",
          "1418964",
          "3001556265",
          "9021987",
          "3009077524",
          "9680825",
          "3002707445",
          "3006115340",
          "2529454",
          "3002532594",
          "1317307",
          "3003768277"
        ],
        "fei_number": [
          "1000121475",
          "3001451453",
          "2431224",
          "3000126629",
          "3002808157",
          "3000204334",
          "3003768251",
          "3002807880",
          "1450835",
          "3008141750",
          "3016674288",
          "1418964",
          "3008656742",
          "3001556265",
          "3002807827",
          "3009077524",
          "3002707445",
          "3006115340",
          "3002532594",
          "1317307"
        ],
        "device_name": "Grid, Radiographic",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.1910",
        "device_class": "1"
      }
    }
  ]
}