{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Vernon Hills",
      "address_1": "75 N Fairway Dr",
      "reason_for_recall": "The integrity of the sterile packaging is potentially compromised.",
      "address_2": "",
      "product_quantity": "a.) 13,010 units b.) 2116 units",
      "code_info": "Product Code: a.) TIN3015/ LOT 0000836578, 0000841213, 0000841215, 0000842719, 0000842721, 0000845423, 0000848061, 0000849715, 0000850938, 0000852076, 0000854859; Product Code: b.) TIN3018/ LOT 0000836574, 0000841212, 0000852078",
      "center_classification_date": "20180418",
      "distribution_pattern": "Nationwide, Australia, Brazil, Canada, China, Japan, Kuwait, Malaysia, Mexico, Netherlands, New Zealand, Philippines, Singapore, South Africa, Taiwan, Thailand, United Arab Emirates, Vietnam",
      "state": "IL",
      "product_description": "ILLINOIS (TJ) NEEDLE ASPIRATION [15GA, 18GA]; STERILE;",
      "report_date": "20180425",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Carefusion 2200 Inc",
      "recall_number": "Z-1423-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76620",
      "termination_date": "20190709",
      "more_code_info": "",
      "recall_initiation_date": "20170223",
      "postal_code": "60061-1845",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}