{
  "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": "Shirley",
      "address_1": "One Luitpold Drive",
      "reason_for_recall": "Presence of Particulate Matter:  In the course of inspecting retention samples visual particles were observed.",
      "address_2": "P.O. Box 9001",
      "product_quantity": "30 mL: 2,078,800 vials; 100 mL: 167,100 vials",
      "code_info": "30 mL  Lots: 9198, 9252, 9299, 9305, 9402, 9423,  9432, 9553, 9595, 9646, 9681, 9737, 9797, 9831, 0051, 0095,  0362;    100 mL  Lots: 9225, 9492, 9711, 0007, 0058",
      "center_classification_date": "20120614",
      "distribution_pattern": "Nationwide, Puerto Rico, and Abu Dhabi",
      "state": "NY",
      "product_description": "CONCENTRATED SODIUM CHLORIDE INJECTION, USP, 23.4%  a) 30 mL SINGLE DOSE VIAL,  (NDC 0517-2930-25), b) 100 mL PHARMACY BULK PACKAGE (NDC 0517-2900-25), Rx Only, AMERICAN REGENT, INC. SHIRLEY, NY 11967.",
      "report_date": "20120620",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Luitpold Pharmaceuticals, Inc.",
      "recall_number": "D-1378-2012",
      "initial_firm_notification": "Press Release",
      "product_type": "Drugs",
      "event_id": "58410",
      "termination_date": "20180628",
      "more_code_info": "",
      "recall_initiation_date": "20110315",
      "postal_code": "11967-9001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}