{
  "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": "2026-07-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Reno",
      "state": "NV",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "69135",
      "recalling_firm": "Solace International Inc",
      "address_1": "80 Continental Dr Ste 101",
      "address_2": "N/A",
      "postal_code": "89509-3440",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "Amazon US and Amazon UK",
      "recall_number": "D-1586-2014",
      "product_description": "Dermatend Ultra, mole, wart and skin tag remover, For external use only, Ingredient: Distilled Water, Sanguinaria Canadensis, Vegetable Glycerin, Butter of Zinc, Germall Plus, 0.34 OZ (10g) container, Solace International, Inc., Reno, NV 89509, USA",
      "product_quantity": "1249 containers and kits",
      "reason_for_recall": "Labeling: Labeling Bears Unapproved Claims; Dermatend is not FDA approved and therefore has not been shown to be safe and effective for the uses suggested in the labeling.",
      "recall_initiation_date": "20140828",
      "center_classification_date": "20140916",
      "termination_date": "20151117",
      "report_date": "20140924",
      "code_info": "All lots",
      "more_code_info": ""
    }
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}