{
  "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": "32007",
      "product_res_number": "Z-0724-04",
      "event_date_initiated": "2004-02-23",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-12-02",
      "res_event_number": "28501",
      "product_code": "CEW",
      "k_numbers": [
        "K013566"
      ],
      "product_description": "IMMULITE 2000 Intact PTH kit",
      "code_info": "Kit lots L2KPP 117 (exp date Aug 31 2004) and 118 (exp date Oct 31 2004)",
      "firm_fei_number": "3005250747",
      "recalling_firm": "Diagnostic Products Corp",
      "address_1": "5700 W 96th St",
      "city": "Los Angeles",
      "state": "CA",
      "postal_code": "90045-5544",
      "additional_info_contact": "Marisa L. Meeks\n310-645-8200 Ext. 2006",
      "reason_for_recall": "High bias noted in samples collected with EDTA. Indication is to not run samples with EDTA.",
      "root_cause_description": "Other",
      "action": "Recall was by letter mailed / faxed on February 23, 2004. Users are instructed to remove EDTA plasma samples for consideration for testing and correct instructions in the package insert.",
      "product_quantity": "2416 kits",
      "distribution_pattern": "North America, Central America, South America, Europe, Asia, South Africa, Middle East.\n\nDomestic includes:\nVA Hospital, St. Louis MO\nVA Medical Center, Denver, CO\nVA Medical Center, Richmond, VA\nVA Medical Center, West Haven, CT\nWalter Reed Army Medical Center, Washington DC",
      "openfda": {
        "k_number": [
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          "K896294",
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          "K163658",
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          "K930008",
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          "K011505",
          "K950211",
          "K070391",
          "K952199",
          "K063605",
          "K831069",
          "K954418",
          "K772249",
          "K901711",
          "K903130",
          "K001411",
          "K033727",
          "K231927",
          "K840379",
          "K813203",
          "K992105",
          "K031534",
          "K811566",
          "K060348",
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          "K051810",
          "K033426",
          "K830664",
          "K942369",
          "K070709",
          "K853784",
          "K831470",
          "K232791",
          "K121981",
          "K820228",
          "K830700",
          "K843870"
        ],
        "registration_number": [
          "2432235",
          "9612316",
          "8031673",
          "2182595",
          "2245285",
          "3022178699",
          "8023018",
          "2020726",
          "3005529799",
          "3002642396",
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          "2517506",
          "1222302",
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          "3000308930",
          "1319681",
          "3005333358",
          "3002800697",
          "2032839",
          "3012963943",
          "2025099",
          "3033967997"
        ],
        "fei_number": [
          "3002808328",
          "2432235",
          "2182595",
          "3002806559",
          "3022178699",
          "2245285",
          "2020726",
          "1000206808",
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          "3002809144",
          "3007111389",
          "3006198300",
          "3009518015",
          "1219913",
          "3011989923",
          "1036362",
          "3002485711",
          "3004185580",
          "1000121039",
          "2122870",
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          "3002806944",
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          "3007118747",
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          "2967",
          "3005333358",
          "3002800697",
          "3012963943",
          "3002806557",
          "3007019572",
          "3033967997"
        ],
        "device_name": "Radioimmunoassay, Parathyroid Hormone",
        "medical_specialty_description": "Clinical Chemistry",
        "regulation_number": "862.1545",
        "device_class": "2"
      }
    }
  ]
}