{
  "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": "El Paso",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "62900",
      "recalling_firm": "Carefusion 213, Llc",
      "address_1": "1550 Northwestern Dr",
      "address_2": "N/A",
      "postal_code": "79912-8000",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "IL, MO, and NJ",
      "recall_number": "D-004-2013",
      "product_description": "ChloraPrep One-Step (2% w/v chlorhexidine gluconate and 70% v/v isopropyl alcohol) Patient Preoperative Skin Preparation, 3mL Applicators, 25 Applicators per Carton, Single Use, Latex Free, Applicator is STERILE if package is intact, NDC 54365-400-01.",
      "product_quantity": "576 Cartons",
      "reason_for_recall": "Lack of Assurance of Sterility: Firm mistakenly released quarantined, non conforming material that failed sterility testing.",
      "recall_initiation_date": "20120423",
      "center_classification_date": "20121003",
      "termination_date": "20130911",
      "report_date": "20121010",
      "code_info": "Lot 52894, Product Code: 260400"
    }
  ]
}