{
  "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": "Lincoln",
      "address_1": "10401 Hwy 6",
      "reason_for_recall": "Presence of Foreign Substance: The products are being recalled because they may contain foreign substances.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Lot #: a) 10119730, Exp 9/30/2013; b) 10115568, 10115570, Exp 6/30/2013; 10119728, Exp 9/30/2013.",
      "center_classification_date": "20140117",
      "distribution_pattern": "Nationwide, Mexico, Russia, Korea, Panama, China, and Canada.",
      "state": "NE",
      "product_description": "Theraflu Exte (dextromethorphan hydrobromide 20 mg, phenylephrine hydrochloride 20 mg, chlorpheniramine maleate 10 mg) powder packets, lemon flavor, packaged in a) 6-count packets per carton (UPC 7 501124 812881) and b) 10-count packets per carton (UPC 7 501124 814595), Distributed by Novartis Farmaceutica, S.A., DE C.V., Mexico.",
      "report_date": "20140129",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Novartis Consumer Health",
      "recall_number": "D-762-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "65490",
      "termination_date": "20141104",
      "more_code_info": "",
      "recall_initiation_date": "20130618",
      "postal_code": "68517-9626",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}