{
  "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": "2026-08-15",
    "results": {
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  "results": [
    {
      "cfres_id": "35979",
      "product_res_number": "Z-0297-05",
      "event_date_initiated": "2004-11-05",
      "event_date_posted": "2004-12-08",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-08-29",
      "res_event_number": "30483",
      "product_code": "NPQ",
      "product_description": "MagNA Pure LC Instrument; catalog numbers 2236931 and 03670325001.",
      "code_info": "All systems using software version 3.09.",
      "firm_fei_number": "1823260",
      "recalling_firm": "Roche Diagnostics Corp.",
      "address_1": "9115 Hague Rd",
      "city": "Indianapolis",
      "state": "IN",
      "postal_code": "46256-1025",
      "additional_info_contact": "800-526-1247",
      "reason_for_recall": "Test results may be adversely affected by software shutting down the cooling blocks in systems with software version 3.09.",
      "root_cause_description": "Other",
      "action": "Consignees were notified via letter dated 11/5/04, which provides the user with a workaround.",
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        "device_name": "Test, Factor V Leiden Mutations, Genomic Dna Pcr",
        "medical_specialty_description": "Hematology",
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