{
  "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": "Rockford",
      "address_1": "4901 Hiawatha Dr",
      "reason_for_recall": "Subpotent Drug and Failed Impurities/Degradation Specifications",
      "address_2": "",
      "product_quantity": "78,090 vials",
      "code_info": "Lot #: UW301, UW302, Exp 02/15; UW303, UW304, UW305, UW306, Exp 04/15",
      "center_classification_date": "20150316",
      "distribution_pattern": "Nationwide",
      "state": "IL",
      "product_description": "Nicardipine Hydrochloride Injection, 25 mg/10 ml (2.5 mg/mL),10 mL single dose vial, Rx only, Manufactured in India for: Mylan Institutional LLC, Rockford, IL 61103, NDC 67457-224-10",
      "report_date": "20150325",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Mylan Institutional LLC",
      "recall_number": "D-0413-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "70375",
      "termination_date": "20160411",
      "more_code_info": "",
      "recall_initiation_date": "20150123",
      "postal_code": "61103-1287",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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  ]
}