{
  "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": "Dubai",
      "state": "N/A",
      "country": "United Arab Emirates",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "69370",
      "recalling_firm": "Sun Pharma Global Inc.",
      "address_1": "P.O. Box 12850",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide and Puerto Rico",
      "recall_number": "D-0236-2015",
      "product_description": "Venlafaxine Hydrochloride Extended-Release Tablets, 37.5 mg, 30-count bottles and 90-count bottles, RX only, Manufactured for Sun Pharma Global Inc. Dubai, United Arab Emirates by Sun Pharmaceutical Industries Limited, Halol, India",
      "product_quantity": "68194",
      "reason_for_recall": "Failed Dissolution Specifications; 12 month stability time point",
      "recall_initiation_date": "20140926",
      "center_classification_date": "20141104",
      "termination_date": "20150506",
      "report_date": "20141112",
      "code_info": "Batch Number: JKM3855A  Mfg. Date: 06/25/2013  Exp. Date: 05/31/2015    Batch Number: JKM3855B  Mfg. Date: 06/25/2013  Exp. Date: 05/31/2015    Batch Number: JKM7265A  Mfg. Date: 12/25/2013  Exp. Date: 11/30/2015    Batch Number: JKM7265B  Mfg. Date: 12/25/2013  Exp. Date: 11/30/2015"
    }
  ]
}