{
  "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": "Brea",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "80277",
      "recalling_firm": "BioDiagnostic International",
      "address_1": "555 W Lambert Rd Ste C",
      "address_2": "N/A",
      "postal_code": "92821-3917",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed to one sole customer in Illinois who further distributed Nationwide in the USA.",
      "recall_number": "D-0874-2018",
      "product_description": "Monsel's Solution (Ferric Subsulfate), 20%, packaged as 12 single application vials and 12 applicators, 8 mL per box, Manufactured For: MedGyn Products, Inc., 100 W. Industrial Rd., Addison, IL  60101 USA; Manufactured By: BioDiagnostics Intl, 555 West Lambert Road Unit-C, Brea, CA  92821, NDC 42721-112-08.",
      "product_quantity": "1000 boxes",
      "reason_for_recall": "CGMP Deviations: Products not manufactured under current good manufacturing practices.",
      "recall_initiation_date": "20180611",
      "center_classification_date": "20180614",
      "termination_date": "20190725",
      "report_date": "20180620",
      "code_info": "All lots within expiry"
    }
  ]
}