{
  "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": {
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  "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",
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      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0406-2024",
      "product_description": "HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride, (Concentration = 0.2mg/ml) 30 mL Syringe, Rx only, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT 06095,  NDC 70004-0300-18, Bar Code 70004030018",
      "product_quantity": "1,425 syringes",
      "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 #: 1223048451 Exp 11/20/23; 1223048923 Exp 12/07/23; 1223049097 Exp 12/15/23; 1223049129 Exp 12/19/23;",
      "more_code_info": ""
    }
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}