{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Pithampur",
      "state": "N/A",
      "country": "India",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "77323",
      "recalling_firm": "Lupin Limited (Unit 1)",
      "address_1": "Unit 1, Plot 2, SEZ, Phase II,",
      "address_2": "Misc Zone Apparel Park, Dist. Dhar",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1093-2017",
      "product_description": "Mibelas 24 Fe (Norethindrone acetate and Ethinyl estradiol 1 mg/0.02 mg chewable and ferrous Fumarate 75 mg) Tablets, wallet of 28 tablets (NDC 68180-911-11), Carton of 3 wallets (NDC 68180-911-13), Rx Only, Manufactured by: Lupin Limited, India, Distributed by Lupin Pharmaceuticals, Inc., Baltimore, MD, 21202",
      "product_quantity": "24,652 tablets",
      "reason_for_recall": "Contraceptive Tablets Out of Sequence- First 4 pills of the packet are brown, instead of the last four pills and the expiry/lot was not printed on the package.",
      "recall_initiation_date": "20170516",
      "center_classification_date": "20170815",
      "termination_date": "20190530",
      "report_date": "20170823",
      "code_info": "Batch Number L600518; Exp. 05/18"
    }
  ]
}