{
  "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": "South San Francisco",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "64151",
      "recalling_firm": "Actelion Pharmaceuticals U.S., Inc.",
      "address_1": "5000 Shoreline Ct. Ste 200",
      "address_2": "N/A",
      "postal_code": "94080-1956",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA & VA",
      "recall_number": "D-143-2013",
      "product_description": "Ventavis (iloprost) Inhalation Solution, 10 mcg/1 mL, Sterile, 30 Single Use Ampules per carton, Manufactured for Actelion Pharmaceuticals US, Inc, 5000 Shoreline Court, Ste 200, South San Francisco, CA 94080, NDC: 66215-302-30.",
      "product_quantity": "3 Cartons",
      "reason_for_recall": "Subpotent Drug: OOS (out of specification) assay result at the 12 month stability time point.",
      "recall_initiation_date": "20130116",
      "center_classification_date": "20130201",
      "termination_date": "20130723",
      "report_date": "20130213",
      "code_info": "Lot #: MA00AD5, Exp: 11/30/2014",
      "more_code_info": ""
    }
  ]
}