{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Sharm",
      "state": "N/A",
      "country": "United Arab Emirates",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "70339",
      "recalling_firm": "Sun Pharma Global Fze",
      "address_1": "Office # 43 Block Y Saif Zone",
      "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.",
      "recall_number": "D-0386-2015",
      "product_description": "Levetiracetam, extended release tablets, 750 mg, 60-count bottle, Rx only, Manufactured by Sun Pharmaceutical Ind. Ltd Halol-Baroda Highway, Halol-389 350, Gujarat, India,   NDC Number: 47335-576-86",
      "product_quantity": "3263 bottles",
      "reason_for_recall": "Failed Dissolution Specifications: 6 month time point.",
      "recall_initiation_date": "20150121",
      "center_classification_date": "20150212",
      "termination_date": "20151023",
      "report_date": "20150218",
      "code_info": "Lot #: JKN0249A Exp 02/2016"
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}