{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Woodland Hills",
      "address_1": "6400 Canoga Ave",
      "reason_for_recall": "EEG Info, Inc. is recalling the EEG Neuroamp device because they have identified a potential risk associated with the mislabeling of certain devices.",
      "address_2": "Suite 210",
      "product_quantity": "1308 units",
      "code_info": "Serial Number: 0001-3343.",
      "center_classification_date": "20121217",
      "distribution_pattern": "Nationwide Distribution",
      "state": "CA",
      "product_description": "EEG NeuroAmp, Model Number: CS 10090; CS 10137.    Biofeedback and Relaxation",
      "report_date": "20121226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "EEG Info",
      "recall_number": "Z-0526-2013",
      "initial_firm_notification": "Letter",
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      "recall_initiation_date": "20121115",
      "postal_code": "91367-2425",
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