{
  "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": [
    {
      "status": "Terminated",
      "city": "Lake Forest",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "64482",
      "recalling_firm": "Hospira Inc.",
      "address_1": "275 N Field Dr",
      "address_2": "N/A",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-206-2013",
      "product_description": "METRONIDazole Injection, USP 500 mg (5 mg/mL), 100 mL Bag,  Rx only, Hospira, Inc. Lake Forest, IL 60045 (NDC 0409-7811-24)",
      "product_quantity": "567,624 bags",
      "reason_for_recall": "Lack of Assurance of Sterility: There is the potential for the solution to leak from the administrative port to the fill tube seal.",
      "recall_initiation_date": "20130215",
      "center_classification_date": "20130321",
      "termination_date": "20150331",
      "report_date": "20130327",
      "code_info": "Lot code 12-074-JT Exp 12/13"
    }
  ]
}