{
  "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": [
    {
      "status": "Terminated",
      "city": "Lincolnton",
      "state": "NC",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "62827",
      "recalling_firm": "Actavis Mid Atlantic LLC",
      "address_1": "1877 Kawai Rd",
      "address_2": "N/A",
      "postal_code": "28092-5905",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide & Puerto Rico",
      "recall_number": "D-006-2013",
      "product_description": "Prometh VC with Codeine Cough Syrup, CV, Each 5mL contains: Codeine phosphate 10mg; promethazine hydrochloride 6.25mg; phenylephrine hydrochloride 5mg, One Pint Bottles (473mL), Rx Only, Manufactured by: Actavis Mid Atlantic LLC., 1877 Kawaii Road, Lincolnton, NC 28092 USA, NDC 0472-1629-16",
      "product_quantity": "19,980 Bottles",
      "reason_for_recall": "Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.",
      "recall_initiation_date": "20120814",
      "center_classification_date": "20121009",
      "termination_date": "20130627",
      "report_date": "20121017",
      "code_info": "X110042, X110051, X110064, Exp 09/13"
    }
  ]
}