{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "El Paso",
      "address_1": "1550 Northwestern Drive",
      "reason_for_recall": "Labeling: Not Elsewhere Classified: This product is misbranded because the product is not sterile and the labeling is misleading in relation to sterility claims.",
      "address_2": "",
      "product_quantity": "8,960,000 applicators",
      "code_info": "a) All lots with expiry between 09/12 to 10/15 and b) All lots with expiry between 10/11 to 07/14.",
      "center_classification_date": "20130328",
      "distribution_pattern": "Nationwide, Puerto Rico, Virgin Islands, Malaysia, and United Kingdom",
      "state": "TX",
      "product_description": "SEPP 10% Povidone Iodine Solution USP (1% available Iodine, Surfactant & USP Purified Water), packaged in a) 200-count applicators (Net 0.67 mL each) per carton, CareFusion, Leawood, KS  66211, Cat. No 260286, NDC 54365-145-01; and b) 3000-count applicators per case, Cat. No 260681, CareFusion, Leawood, KS  66211.",
      "report_date": "20130403",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CareFusion 213, LLC",
      "recall_number": "D-226-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "64583",
      "termination_date": "20140512",
      "more_code_info": "",
      "recall_initiation_date": "20130304",
      "postal_code": "79912-8000",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}