{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Salisbury",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "64869",
      "recalling_firm": "Jubilant Cadista Pharmaceuticals Inc.",
      "address_1": "207 Kiley Dr",
      "address_2": "",
      "postal_code": "21801-2249",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-296-2013",
      "product_description": "Pantoprazole Sodium Delayed Release Tablets USP, 40 mg, 90 count bottles, Manufactured by Jubilant Life Sciences Ltd, Roorkee-247661 India ;Marketed by Jubilant Cadista Pharmaceuatical Inc Salisbury, MD 21801 NDC 59746-284-90",
      "product_quantity": "12770 bottles",
      "reason_for_recall": "cGMP Deviations: Oral products were not manufactured in accordance with Good Manufacturing Practices.",
      "recall_initiation_date": "20130211",
      "center_classification_date": "20130426",
      "termination_date": "20131223",
      "report_date": "20130508",
      "code_info": "Lot PA22028 Exp 5/2014  Lot PA22029 Exp 5/2014",
      "more_code_info": ""
    }
  ]
}