{
  "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": "Santa Ana",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "63095",
      "recalling_firm": "Dispensing Solutions, Inc",
      "address_1": "3000 W Warner Ave",
      "address_2": "N/A",
      "postal_code": "92704-5311",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US:  IN & WI",
      "recall_number": "D-1691-2012",
      "product_description": "Atrovent HFA Inhalation Aerosol, (ipratropium bromide) 12.9 grams, 200 metered actuations, Rx only, Packaged Exclusively by: Dispensing Solutions, Inc., Santa Ana, CA --- NDC 68258-8952-01, DSI product #8A0947",
      "product_quantity": "18 Inhalers",
      "reason_for_recall": "Label Mix up; side panel of sticker label applied by Dispensing Solutions Inc. incorrectly indicates product name as Ventolin HFA 90 mcg instead of correctly as Atrovent HFA 12.9 grams Inhalation Aerosol",
      "recall_initiation_date": "20120828",
      "center_classification_date": "20120925",
      "termination_date": "20121101",
      "report_date": "20121003",
      "code_info": "Lot # F23989, F22311",
      "more_code_info": ""
    }
  ]
}