{
  "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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      "product_res_number": "Z-0055-2008",
      "event_date_initiated": "2007-08-03",
      "event_date_posted": "2007-10-12",
      "recall_status": "Terminated",
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      "res_event_number": "39383",
      "product_code": "LGW",
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      "product_description": "Precision Implantable Pulse Generator (IPG), Model Number SC-110",
      "code_info": "Model Number SC-1110, Serial Number 161767",
      "firm_fei_number": "1000220815",
      "recalling_firm": "Advanced Bionics Corp",
      "address_1": "12740 San Fernando Rd",
      "city": "Sylmar",
      "state": "CA",
      "postal_code": "91342-3728",
      "additional_info_contact": "Kaoru Lee Adair\n818-362-1669",
      "reason_for_recall": "Mislabeled: Product labeled with the incorrect shelf-life information.",
      "root_cause_description": "Error in labeling",
      "action": "There was one unit affected by this field action. An Advanced Bionics representative contacted and visited the facility on August 3, 2007. At this time, the affected device has been retrieved by the Company.",
      "product_quantity": "1 unit affected",
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        "medical_specialty_description": "Unknown",
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}