{
  "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": "2026-04-08",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "New York",
      "address_1": "Apartment 16",
      "reason_for_recall": "Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation",
      "address_2": "241 West 36th Street",
      "product_quantity": "30 units",
      "code_info": "none",
      "center_classification_date": "20180301",
      "distribution_pattern": "US Nationwide",
      "state": "NY",
      "product_description": "Truth Renew",
      "report_date": "20180307",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Accord Media, LLC",
      "recall_number": "Z-0820-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79262",
      "termination_date": "20200528",
      "recall_initiation_date": "20171204",
      "postal_code": "10018",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}