{
  "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": "Davie",
      "state": "FL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "71755",
      "recalling_firm": "Actavis Laboratories, FL, Inc.",
      "address_1": "4955 Orange Dr",
      "address_2": "N/A",
      "postal_code": "33314-3902",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "U.S. Nationwide including Puerto Rico.",
      "recall_number": "D-1285-2015",
      "product_description": "Desmopressin Acetate Tablets, 0.1mg, 100 Count Bottles, Rx Only. Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA; Distributed by Actavis Pharma, Inc. Parsippany, NJ 07054 USA.  NDC: 0591-2464-01.",
      "product_quantity": "11,445 Bottles",
      "reason_for_recall": "Tablets/Capsules Imprinted with Wrong ID: Some tablets incorrectly imprinted with an X on one side.",
      "recall_initiation_date": "20150623",
      "center_classification_date": "20150804",
      "termination_date": "20161230",
      "report_date": "20150812",
      "code_info": "Lot # 982021M, Expiry: DEC. 2016"
    }
  ]
}