{
  "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; white substance confirmed as Guaifenesin, an active ingredient was observed in some bottles.  If the product is shaken or warmed the white particles goes into the solution.",
      "address_2": "11840 S Alameda ST",
      "product_quantity": "5,676 bottles (473 cases)",
      "code_info": "Lot# 71648, 68088;  FP-47-041-02535",
      "center_classification_date": "20130307",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "Select Brand Cough Control CF Max, Maximum Strength for MUCUS RELIEF, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 4 fl.oz 12pk (NDC 15127-025-04; UPC Code: 0-15127-02535-5), Distributed by: Select Brand Distributors, Pine Bluff, AR 71603 USA.",
      "report_date": "20130313",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Aaron Industries Inc",
      "recall_number": "D-187-2013",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Drugs",
      "event_id": "64298",
      "termination_date": "20131101",
      "recall_initiation_date": "20130118",
      "postal_code": "90262-4022",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}