{
  "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": [
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      "cfres_id": "36004",
      "product_res_number": "Z-0396-05",
      "event_date_initiated": "2004-11-11",
      "event_date_posted": "2005-01-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-03-08",
      "res_event_number": "30494",
      "product_code": "LGW",
      "pma_numbers": [
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      "product_description": "Charger Assembly, Model # SC-5300, of the PRECISION Spinal Cord Stimulation System",
      "code_info": "All Codes",
      "firm_fei_number": "1000220815",
      "recalling_firm": "Advanced Bionics Corporation",
      "address_1": "12740 San Fernando Rd",
      "city": "Sylmar",
      "state": "CA",
      "postal_code": "91342-3728",
      "additional_info_contact": "Kay Adair\n661-362-1669",
      "reason_for_recall": "A burn injury was sustained by a patient that did not follow the directions for use and also slept while charging the unit.",
      "root_cause_description": "Other",
      "action": "Firm has notified all consignees and thier clinicians to provide them with the labeling addenda. Patient notices were sent by FedEx or by US Mail and clinicians were faxed the notice.",
      "product_quantity": "237 patients are implanted.",
      "distribution_pattern": "Nationwide",
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        "device_name": "Stimulator, Spinal-Cord, Totally Implanted For Pain Relief",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
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    }
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}