{
  "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": {
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      "cfres_id": "36062",
      "product_res_number": "Z-0324-05",
      "event_date_initiated": "2004-11-19",
      "event_date_posted": "2004-12-17",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-03-24",
      "res_event_number": "30530",
      "product_code": "CFP",
      "product_description": "Immulite 2500 insulin Kit",
      "code_info": "lot 102A",
      "firm_fei_number": "3005250747",
      "recalling_firm": "Diagnostic Products Corp",
      "address_1": "5210 Pacific Concourse Dr",
      "city": "Los Angeles",
      "state": "CA",
      "postal_code": "90045-6900",
      "additional_info_contact": "Steve Iland\n310-645-8200 Ext. 7434",
      "reason_for_recall": "Low bias of 10 to 40% at different levels of insulin in samples.",
      "root_cause_description": "Other",
      "action": "Customers were notified by telephone on 11/19/2004. They were instructed to discard remaining kits.",
      "product_quantity": "10 kits",
      "distribution_pattern": "Medical facilities in AK, NY, WI.",
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        "device_name": "Radioimmunoassay, Immunoreactive Insulin",
        "medical_specialty_description": "Clinical Chemistry",
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