{
  "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": "2026-10-14",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 32
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Windsor",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "86990",
      "recalling_firm": "SCA Pharmaceuticals",
      "address_1": "755 Rainbow Rd Ste B",
      "address_2": "",
      "postal_code": "06095-1024",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed to hospitals nationwide.",
      "recall_number": "D-0215-2021",
      "product_description": "HYDROmorphone HCl 10mg/50mL in 0.9% Sodium Chloride Injection, CII, Rx Only, 50 mL Single Dose Syringe, SCA Pharmaceuticals, 755 Rainbow Rd., Windsor, CT, 06095, barcode 70004030022",
      "product_quantity": "428 syringes",
      "reason_for_recall": "Lack of Assurance of Sterility; potential for a defective syringe cap, resulting in a non-integral unit",
      "recall_initiation_date": "20201217",
      "center_classification_date": "20210107",
      "termination_date": "20211102",
      "report_date": "20210113",
      "code_info": "Lot #    1220023220, BUD 1/31/2021;  1220023337, BUD 2/2/2021 &  1220023443, BUD 2/22/2021.",
      "more_code_info": ""
    }
  ]
}