{
  "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": "6,108 bottles (509 cases)",
      "code_info": "Lot# 80798;  FP-49-081-14870,",
      "center_classification_date": "20130307",
      "distribution_pattern": "Nationwide",
      "state": "CA",
      "product_description": "Well at Walgreens Wal-Tussin CF Max, MAXIMUM STRENGTH ADULT NON-DROWSY, Multi-Symptom Cold, (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCI 5 mg), 8 FL OZ (237 mL) bottles, Distributed by: Walgreen Co, Deerfield, IL 60015 ----  NDC 0363-0229-08",
      "report_date": "20130313",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Aaron Industries Inc",
      "recall_number": "D-185-2013",
      "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"
    }
  ]
}