{
  "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": "Alpharetta",
      "state": "GA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "77605",
      "recalling_firm": "Shionogi Inc.",
      "address_1": "5770 Shiloh Rd",
      "address_2": "N/A",
      "postal_code": "30005-8408",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0982-2017",
      "product_description": "PONSTEL (Mefanamic Acid) USP, 250 mg capsules, 30-count bottles, Rx Only, Manufactured for: Shionogi Inc. Florham Park, NJ 07932 Manufactured by: Halo Pharmaceutical Inc. Whippany, NJ 07981",
      "product_quantity": "455 bottles",
      "reason_for_recall": "Failed Dissolution Specifications: Low dissolution results were obtained during stability testing",
      "recall_initiation_date": "20170524",
      "center_classification_date": "20170714",
      "termination_date": "20180228",
      "report_date": "20170726",
      "code_info": "Lot #: 5H66200103, Exp. June 2018"
    }
  ]
}