{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Nashville",
      "address_1": "5209 Linbar Dr",
      "reason_for_recall": "One lot of 0.9% Sodium Chloride Flush syringe, 3 mL in 12 mL may be mislabeled as 0.9% Sodium Chloride Flush syringe, 10 mL in 12 mL.",
      "address_2": "Suite 640",
      "product_quantity": "196,400 units",
      "code_info": "KH03752",
      "center_classification_date": "20120915",
      "distribution_pattern": "Distributed to one customer in Illinois.",
      "state": "TN",
      "product_description": "0.9% Sodium Chloride Injection, USP, Pre-Filled Flush Solution, 3 mL in 12 mL Single Use Syringe, Rx only, List no. 1078-33, made in Nashville, TN, manufactured for Hospira, Inc., Lake Forest, IL  60045 USA.    Flush syringe.",
      "report_date": "20120926",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Amsino Medical USA",
      "recall_number": "Z-2393-2012",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "63105",
      "termination_date": "20130813",
      "more_code_info": "",
      "recall_initiation_date": "20120815",
      "postal_code": "37211-1026",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}