{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plano",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69025",
      "recalling_firm": "St. Jude Medical, Inc.",
      "address_1": "6901 Preston Rd",
      "address_2": "N/A",
      "postal_code": "75024-2508",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in the states of Texas and Illinois.",
      "recall_number": "Z-2718-2014",
      "product_description": "Percutaneous Trial Lead Kit Model 3046 (4 ch percutaneous lead).    Used as part of the St. Jude Medical Neurostimulation system indicated for Spinal Chord Stimulation.",
      "product_quantity": "2 units",
      "reason_for_recall": "The Directions for Use (DFU) manual contains information for devices that are not approved in the US.  The correct US approved versions of the manuals were sent to the customers to replace the incorrect international manuals.",
      "recall_initiation_date": "20140729",
      "center_classification_date": "20140929",
      "termination_date": "20150821",
      "report_date": "20141008",
      "code_info": "Material 100077113, Batch 4558337"
    }
  ]
}