{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "Bennet",
      "state": "NE",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "95503",
      "recalling_firm": "Staska Pharmaceuticals, Inc.",
      "address_1": "742 Evergreen Dr",
      "address_2": "N/A",
      "postal_code": "68317-2365",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0040-2025",
      "product_description": "Ascorbic Acid Inj. Solution, 25,000mg/50mL (500mg/mL), 50mL single use vial, Rx only, Staska Pharmaceuticals, 742 Evergreen Drive, Bennet, NE 68317",
      "product_quantity": "4773 vials",
      "reason_for_recall": "Presence of Particulate Matter: Presence of glass particulates.",
      "recall_initiation_date": "20240930",
      "center_classification_date": "20241107",
      "termination_date": "20250805",
      "report_date": "20241113",
      "code_info": "Lot #SP2400058, Exp 12/31/2024",
      "more_code_info": ""
    }
  ]
}