{
  "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": "Mehbubnagar",
      "state": "N/A",
      "country": "India",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "62113",
      "recalling_firm": "Aurobindo Pharma LTD",
      "address_1": "Unit VII, Formulation Plant",
      "address_2": "Survey 411, 425, 434-435, 458, Plot S1",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "FAX",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-041-2013",
      "product_description": "Northstar Zolpidem Tartrate Tablets USP 10 mg.  Manufactured for Northstar RX, LLC Memphis, TN 38141.  Manufactured by Aurobindo Pharma Limited, Unit VII, Mahaboob Dagar, 509302, India",
      "product_quantity": "23,616 bottles",
      "reason_for_recall": "Adulterated Presence of Foreign Tablets: This product is being recalled becaiuse 30 valacyclovir hydrochloride tablets USP 500 mg were discovered in a bottle labeled Zolpidem Tartrate tables USP 10 mg",
      "recall_initiation_date": "20120309",
      "center_classification_date": "20121106",
      "termination_date": "20131121",
      "report_date": "20121114",
      "code_info": "Batch Number ZPSB11054-A Exp. 05/13"
    }
  ]
}