{
  "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": "Glasgow",
      "state": "KY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "78035",
      "recalling_firm": "Amneal Pharmaceuticals LLC",
      "address_1": "118 Beaver Trl",
      "address_2": "N/A",
      "postal_code": "42141-1273",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "MS, NC, OH, TX, UT",
      "recall_number": "D-0076-2018",
      "product_description": "Fosphenytoin Sodium Injection, USP,  500 mg  PE/10 mL (50 mg PE/mL.  10 mL Single Dose Vial, Rx Only. Distributed by: Amneal Biosciences, Bridgewater, NJ 08807. NDC: 70121-1390-7",
      "product_quantity": "14,000 vials",
      "reason_for_recall": "Presence of Particulate Matter",
      "recall_initiation_date": "20170831",
      "center_classification_date": "20171113",
      "termination_date": "20190910",
      "report_date": "20171122",
      "code_info": "Lot # AP160016; Exp. 05/18"
    }
  ]
}