{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Draper",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65492",
      "recalling_firm": "Edwards Lifesciences, LLC",
      "address_1": "12050 Lone Peak Pkwy",
      "address_2": "N/A",
      "postal_code": "84020-9414",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and Canada.",
      "recall_number": "Z-1749-2013",
      "product_description": "Edwards Lifesciences Suction Wand, models S099 and S0998B    Suction wands are intended for hand held use and pericardial sumps are intended for stationary use in removing excess fluid from the surgical field.",
      "product_quantity": "S099: 171,587 units and S099B: 505,107 units",
      "reason_for_recall": "Edwards is recalling certain lots of Rigid Suction Wands because they discovered plastic particulate inside the sterile pouch and within the internal diam ether of the wand.",
      "recall_initiation_date": "20130619",
      "center_classification_date": "20130717",
      "termination_date": "20141104",
      "report_date": "20130724",
      "code_info": "Models S099 and S099B"
    }
  ]
}