{
  "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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      "product_res_number": "Z-0002-2007",
      "event_date_initiated": "2006-05-19",
      "event_date_posted": "2006-10-12",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-12-31",
      "res_event_number": "35672",
      "product_code": "LWS",
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      "firm_fei_number": "2124215",
      "recalling_firm": "Guidant Corporation",
      "address_1": "4100 Hamline Ave N",
      "city": "Saint Paul",
      "state": "MN",
      "postal_code": "55112-5700",
      "reason_for_recall": "Final software load did not occur prior to shipment of select programmers.",
      "root_cause_description": "Other",
      "action": "Sales Representatives were asked to retrieve/return identified monitors.",
      "product_quantity": "8",
      "distribution_pattern": "Nationwide distribution --- including states of AR, MI, PA",
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        "medical_specialty_description": "Unknown",
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