{
  "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": "Bridgewater",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "63524",
      "recalling_firm": "Dr. Reddy's Laboratories, Inc.",
      "address_1": "200 Somerset Corporate Blvd Fl 7th",
      "address_2": "N/A",
      "postal_code": "08807-2862",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide.  No foreign consignees.",
      "recall_number": "D-059-2013",
      "product_description": "Dr. Reddy's Quetiapine Fumarate Tablets, 25mg, Rx Only, 500 tablets.    Mfd By: Dr. Reddy's Laboratories Limited, Bachepalli - 502 325, India    NDC 55111-249-05",
      "product_quantity": "1512 bottles",
      "reason_for_recall": "Failed USP Dissolution Test Requirements: During analysis of long term stability studies at 3 months time point, an OOS was reported for Quetiapine Fumarate Tablets, 25 mg.",
      "recall_initiation_date": "20120927",
      "center_classification_date": "20121120",
      "termination_date": "20130710",
      "report_date": "20121128",
      "code_info": "Lot C203090 Exp.03/14"
    }
  ]
}