{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lincoln",
      "state": "RI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "92268",
      "recalling_firm": "Denison Pharmaceuticals, LLC",
      "address_1": "1 Powder Hill Rd",
      "address_2": "N/A",
      "postal_code": "02865-4407",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed Nationwide.",
      "recall_number": "D-0772-2023",
      "product_description": "Safe tussin DM, DAY TIME Cough Relief, (Dextromethorphan HBr, USP 10mg Guaifenesin, USP 100mg), 4.0 FL OZ (118mL) bottle, Kramer Laboratories , Inc. Bridgewater, NJ 08807.",
      "product_quantity": "86,616 4 OZ bottles",
      "reason_for_recall": "CGMP Deviations: Use of non-food grade lubricant in mixing vessel.",
      "recall_initiation_date": "20230503",
      "center_classification_date": "20230531",
      "report_date": "20230607",
      "code_info": "Lot: 8314, Exp: 04/2023, 8753, 8753A, Exp: 10/2023; 8659, Exp: 08-2023"
    }
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}