{
  "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": "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-0416-2024",
      "product_description": "PHENYLephrine HCl 500 mcg/5 mL in 0.9% Sodium Chloride Injection, (Concentration = 100 mcg/mL), 5 mL fill 12 mL Syringe, Rx Only, SCA Pharmaceuticals, 755 Rainbow Rd. Windsor, CT 06095, NDC 70004-0810-11-K, Bar Code 70004081011. (same finished product as F078140, but with RFID for KitCheck",
      "product_quantity": "1,118 syringes in kits",
      "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 #: 1223048431 exp 04/05/24; 1223049023 exp 04/25/24",
      "more_code_info": ""
    }
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}