{
  "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": "Hobart",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "61967",
      "recalling_firm": "Mallinckrodt Inc.",
      "address_1": "172 Railroad Avenue",
      "address_2": "N/A",
      "postal_code": "13788-0416",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1430-2012",
      "product_description": "Hydrocodone Bitartrate and Acetaminophen Oral Solution, 7.5 mg/500 mg per 15 mL, 16 fl oz (473 mL) bottle, Rx only, Mallinckrodt Inc., Hazelwood, MO 63042 USA, NDC 0406-0375-16, UPC 3 0406-0375-16 1.",
      "product_quantity": "41,100 bottles",
      "reason_for_recall": "Subpotent (Multiple Ingredient) Drug: Low out of specification assay results for the hydrocodone bitartrate ingredient was found.",
      "recall_initiation_date": "20120525",
      "center_classification_date": "20120731",
      "termination_date": "20150417",
      "report_date": "20120808",
      "code_info": "Lot #: 0375T79384, Exp 05/13; 0375T81348,  Exp 09/13; 0375U82277, Exp 01/14"
    }
  ]
}