{
  "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": "2026-03-18",
    "results": {
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  "results": [
    {
      "status": "Terminated",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "76472",
      "recalling_firm": "Synergy Rx",
      "address_1": "4901 Morena Blvd Ste 504A",
      "address_2": "N/A",
      "postal_code": "92117-7310",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0570-2017",
      "product_description": "REVERSE DML LOTION (Ketoconazole 2%, Metronidazole 2%, sulfacetamide sodium 10%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676",
      "product_quantity": "N/A",
      "reason_for_recall": "Lack of Assurance of Sterility: There are also CGMP Deviations.",
      "recall_initiation_date": "20170210",
      "center_classification_date": "20170315",
      "termination_date": "20170523",
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      "code_info": "All Lots"
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