{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Windsor",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "93456",
      "recalling_firm": "SCA Pharmaceuticals, LLC",
      "address_1": "755 Rainbow Rd Ste B",
      "address_2": "N/A",
      "postal_code": "06095-1024",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0400-2024",
      "product_description": "fentaNYL 500 mcg/100 mL, Bupivacaine HCl 0.04% in 0.9% Sodium Chloride 100 mL Injection (fentaNYL Concentration = 5 mcg/mL), EPIDURAL USE ONLY, 100 mL Yellow CADD Cassette, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095, NDC 70004-0289-64, Bar Code 70004028964",
      "product_quantity": "412 cassettes",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20231109",
      "center_classification_date": "20240322",
      "termination_date": "20240827",
      "report_date": "20240403",
      "code_info": "Lot #: 1223049261, Exp 12/25/23; 1223049724, Exp 01/11/24",
      "more_code_info": ""
    }
  ]
}