{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Lynwood",
      "address_1": "11865 Alameda St",
      "reason_for_recall": "Presence of Precipitate: Recall is due to complaints of a white substance, confirmed as Guaifenesin, an active ingredient in the product which is precipitating out.",
      "address_2": "",
      "product_quantity": "43,921 bottles",
      "code_info": "Lot #: 151631, Exp 10/15 and 152767, Exp 11/15",
      "center_classification_date": "20140228",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCl 5 mg) per 5 mL, 8 FL OZ (237 mL) bottle, Distributed by: Wal-Mart Stores, Inc., Bentonville, AR  72716, NDC 49035-229-08, UPC 6 81131 03884 3.",
      "report_date": "20140312",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Aaron Industries Inc",
      "recall_number": "D-1097-2014",
      "initial_firm_notification": "Telephone",
      "product_type": "Drugs",
      "event_id": "67434",
      "termination_date": "20141029",
      "more_code_info": "",
      "recall_initiation_date": "20140204",
      "postal_code": "90262-4022",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}