{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
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  "results": [
    {
      "country": "United States",
      "city": "Garner",
      "address_1": "1027 Us Highway 70 W",
      "reason_for_recall": "Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared phenolphthalein and fluoxetine, making EDGE an unapproved drug.",
      "address_2": "Suite 227",
      "product_quantity": "150 bottles",
      "code_info": "Lots: ALL",
      "center_classification_date": "20150504",
      "distribution_pattern": "WV who distributed Nationwide.",
      "state": "NC",
      "product_description": "EDGE Amplified Weight Release capsules, 400 mg, 60-count bottle, Developed by Signature, 1027 Highway 70 W, Suite 227, Garner, NC  27529, UPC 8 52175 00417 4.",
      "report_date": "20150513",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Detox Transforms",
      "recall_number": "D-0977-2015",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Drugs",
      "event_id": "70444",
      "termination_date": "20170123",
      "recall_initiation_date": "20150125",
      "postal_code": "27529-2501",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}