{
  "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": "63285",
      "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",
      "recall_number": "D-178-2013",
      "product_description": "Citalopram tablets USP, 10mg, 30-count bottle,  Rx only, Manufactured by Dr. Reddy's Laboratories Limited, Bachupalli,  India 502 325, NDC 55111-342-30",
      "product_quantity": "27,805 bottles",
      "reason_for_recall": "Chemical Contamination: The product is being recalled due to complaints reporting a strong garlic odor or strong chemical smell.",
      "recall_initiation_date": "20120801",
      "center_classification_date": "20130228",
      "termination_date": "20130524",
      "report_date": "20130306",
      "code_info": "Lot #: C201028, Exp 12/13"
    }
  ]
}