{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Windsor",
      "address_1": "755 Rainbow Rd Ste B",
      "reason_for_recall": "Lack of Assurance of Sterility: SCA is conducting a voluntary recall of certain lots of sterile admixtures due to a potential for leakage.",
      "address_2": "",
      "product_quantity": "2,869 bags",
      "code_info": "Lot # 1218001315, 1218001316, 1218001349, 1218001416, 1218001510, 1218001682, 1218001683, 1218001684, 1218001721, 1218001763, 1218001764, Exp 07/26/2018-08/27/2018",
      "center_classification_date": "20180702",
      "distribution_pattern": "Product was distributed throughout the United States.",
      "state": "CT",
      "product_description": "Diltiazem HCL 1 mg/mL in 125 mL 0.9% Sodium Chloride 100 mL bag (total volume 125 mL) (125 mg), SCA Pharmaceuticals, LLC, Windsor, CT",
      "report_date": "20180711",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "SCA Pharmaceuticals, LLC",
      "recall_number": "D-0897-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "80303",
      "termination_date": "20190204",
      "more_code_info": "",
      "recall_initiation_date": "20180614",
      "postal_code": "06095-1024",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}