{
  "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": "88887",
      "product_res_number": "Z-0849-2010",
      "event_date_initiated": "2010-01-21",
      "event_date_posted": "2010-03-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-01-25",
      "res_event_number": "54641",
      "product_code": "IXR",
      "k_numbers": [
        "K970640"
      ],
      "product_description": "EasyDiagnost.  Multi-functional R/F systems used for general R/F, Fluoroscopy, Radiography and Angiography examinations.",
      "code_info": "Site Numbers:   87031, 101955, 250297, 504826, 505057, 505063, 506644, 539519, 557749, 51711358, and 51711365.",
      "firm_fei_number": "1000524572",
      "recalling_firm": "Philips Medical Systems North America Co.   Phillips",
      "address_1": "22100 Bothell Everett Hwy",
      "city": "Bothell",
      "state": "WA",
      "postal_code": "98021-8431",
      "additional_info_contact": "Philips Healthcare Call Center\n800-722-9377 Ext. 5",
      "reason_for_recall": "Device failed to display appropriate labels indicating Radiation Symbol along with the required wording.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "Urgent - Field Safety Notice letters, dated January 20 & 21, 2010, were sent to customers.  The letter identified the affected products, gave a description of the problem & the hazard involved, stated how to identify affected products, actions to be taken by the customer or user, and actions planned by the firm.  Customers are to make sure that the relevant safety precautions are observed and check their operators console (EEC) if the labeling is present as shown in the drawing.  If the labeling is missing, a Philips rep should be contacted.  For further information or support concerning the issue, a Philips rep should be contacted at 800-722-9377.",
      "product_quantity": "11 units",
      "distribution_pattern": "Devices were distributed through out the US in the following states:\n\nAL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KY, LA, MA, MD, ME, MI, MN, MO, NC, ND, NH, NJ, NM, NY, OH, OK, OR, PA, SC, TX, UT, VA, WA, WI, and WY.",
      "openfda": {
        "k_number": [
          "K950402",
          "K912996",
          "K843926",
          "K911267",
          "K874114",
          "K771293",
          "K905152",
          "K883162",
          "K931563",
          "K943581",
          "K922364",
          "K954356",
          "K883153",
          "K792326",
          "K924326",
          "K920728",
          "K915853",
          "K912741",
          "K965096",
          "K874113",
          "K934574",
          "K840226",
          "K760466",
          "K945842",
          "K883863",
          "K944987",
          "K920742",
          "K965105",
          "K770334",
          "K903422",
          "K792645",
          "K896583",
          "K903395",
          "K870707",
          "K901654",
          "K940721",
          "K920726",
          "K896324",
          "K961022",
          "K912586",
          "K951176",
          "K914417",
          "K854478",
          "K854486",
          "K905153",
          "K860913",
          "K893673",
          "K953557",
          "K781532",
          "K920722",
          "K914165",
          "K850948",
          "K892226",
          "K925175",
          "K840227",
          "K971128",
          "K853175",
          "K905501",
          "K854085",
          "K910838",
          "K905265",
          "K791812",
          "K963851",
          "K911098",
          "K913147",
          "K973039",
          "K880529",
          "K882019",
          "K902989",
          "K970640",
          "K935444",
          "K884531",
          "K953556",
          "K000412",
          "K896119",
          "K950981",
          "K922591"
        ],
        "registration_number": [
          "8022065",
          "3033525986",
          "3002808176",
          "9610903",
          "3013846070",
          "3033527770",
          "3000126629",
          "1223864",
          "8030233",
          "9616014",
          "1225473",
          "3007912863",
          "3003927316",
          "3003768251",
          "3012010520",
          "9613445",
          "3010496070",
          "3004977335",
          "3015276088",
          "3008284470",
          "3009077524",
          "2243057",
          "2529571"
        ],
        "fei_number": [
          "3033525986",
          "3002808176",
          "3013846070",
          "3033527770",
          "1000121370",
          "3000126629",
          "3002807145",
          "3002675731",
          "3007912863",
          "3003927316",
          "3002808139",
          "3003768251",
          "3012010520",
          "1000305755",
          "3001237319",
          "3003434037",
          "3002175190",
          "3010496070",
          "3004977335",
          "3015276088",
          "3008284470",
          "3009077524",
          "2243057"
        ],
        "device_name": "Table, Radiographic, Tilting",
        "medical_specialty_description": "Radiology",
        "regulation_number": "892.1980",
        "device_class": "2"
      }
    }
  ]
}