{
  "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": "2026-08-27",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "26368",
      "product_res_number": "Z-0681-03",
      "event_date_initiated": "2003-03-04",
      "event_date_posted": "2003-03-26",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-09-15",
      "res_event_number": "25690",
      "product_code": "MOI",
      "k_numbers": [
        "K964407"
      ],
      "product_description": "IMx CA 15-3 Reagent Pack, list 6A75-22; this reagent pack contains one 4-mL bottle of Mode 1 Calibrator along with other reagents; Abbott Laboratories, Abbott Park, IL",
      "code_info": "list 6A75-22, lot 90843M200",
      "firm_fei_number": "1415939",
      "recalling_firm": "Abbott Laboratories HPD/ADD",
      "address_1": "100/200 Abbott Park Road",
      "city": "Abbott Park",
      "state": "IL",
      "postal_code": "60064",
      "additional_info_contact": "Abbott Customer Support\n877-422-2688",
      "reason_for_recall": "The CA 15-3 Calibrators may cause depressed values for the CA 15-3 High Control and for patient specimens.",
      "root_cause_description": "Other",
      "action": "Recalled by letter dated 3/4/03.  The accounts were informed of the depressed values for the CA 15-3 High Control and for patient specimens, and were requested to discontinue use and destroy any of the three affected lots found in inventory.",
      "product_quantity": "409 packs",
      "distribution_pattern": "Nationwide  and Ecuador, England, Hong Kong, Chile, Japan, Canada, Singapore, Australia, Pakistan, Argentina, Thailand, Aruba, Korea and Jamaica.",
      "openfda": {
        "k_number": [
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          "K240403",
          "K013984",
          "K033036",
          "K971418",
          "K970695"
        ],
        "device_name": "System, Test, Immunological, Antigen, Tumor",
        "medical_specialty_description": "Immunology",
        "regulation_number": "866.6010",
        "device_class": "2",
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