{
  "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": "544,500 kits",
      "code_info": "All lots with expiry between 07/11 to 08/14.",
      "center_classification_date": "20130328",
      "distribution_pattern": "Nationwide, Puerto Rico, Virgin Islands, Malaysia, and United Kingdom",
      "state": "TX",
      "product_description": "FREPP/SEPP Kit containing 1 FREPP (povidone iodine 2% aqueous solution), Net 1.1 mL and 1 SEPP (povidone iodine 10% USP), Net 0.67 mL per kit, packaged in 20 kits per carton, Cat. No 260288, NDC 54365-202-99, CareFusion, Leawood, KS  66211.",
      "report_date": "20130403",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "CareFusion 213, LLC",
      "recall_number": "D-229-2013",
      "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"
    }
  ]
}