{
  "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": "Wilson",
      "address_1": "4700 Sandoz Dr",
      "reason_for_recall": "Subpotent; Hydrochlorothiazide at the 9 month time point.",
      "address_2": "",
      "product_quantity": "2,491 bottles of 100 tablets each",
      "code_info": "Lot CU0856",
      "center_classification_date": "20131230",
      "distribution_pattern": "Nationwide",
      "state": "NC",
      "product_description": "Fosinopril Sodium and Hydrochlorothiazide Tablets, 10 mg/12.5 mg, Rx Only, 100 Tablets, Sandoz Inc. Princeton, NJ 08540 ---NDC 0185-0341-01,",
      "report_date": "20140108",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Sandoz Inc",
      "recall_number": "D-393-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "66554",
      "termination_date": "20150305",
      "more_code_info": "",
      "recall_initiation_date": "20131011",
      "postal_code": "27893-8143",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}