{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Plano",
      "address_1": "6901 Preston Rd",
      "reason_for_recall": "The firm has received 112 complaints of the Eon Mini IPGs that lost the ability to communicate or recharge due to a workmanship issue resulting in loss of pain relief and subsequent explant.  The firm has determined the cause of these reports to be related to process variances in the positioning of the internal battery and printed circuit board, causing a short, and therefore, prematurely depletin",
      "address_2": "",
      "product_quantity": "25, 255 devices",
      "code_info": "Model Number 3788.  All lots manufactured prior to September 20, 2010.",
      "center_classification_date": "20120710",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and internationally to Argentina, Australia, Austria, Belgium, Brazil, Canada, Colombia, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Greece, India, Ireland, Israel, Italy, Japan, Mexico, Netherlands, Puerto Rico, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Turkey, and United Kingdom.",
      "state": "TX",
      "product_description": "Eon Mini Neurostimulation (IPG) System (Model 3788);    The product is indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs including unilateral or bilateral pain associated with the following: failed back surgery syndrome, intractable low back and leg pain.",
      "report_date": "20120718",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Advanced Neuromodulation Systems Inc.",
      "recall_number": "Z-1983-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "61151",
      "termination_date": "20150724",
      "more_code_info": "",
      "recall_initiation_date": "20111219",
      "postal_code": "75024-2508",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}