{
  "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": [
    {
      "country": "United States",
      "city": "Saint Petersburg",
      "address_1": "970 Lake Carillon Dr",
      "reason_for_recall": "Modification were made to the RENASYS EZ NPWT Systems without a 510(k) or PreMarket Approval notification.",
      "address_2": "Ste 110",
      "product_quantity": "2,142 units",
      "code_info": "Model #'s 66800059, all lots since product launched 01/16/2009",
      "center_classification_date": "20140923",
      "distribution_pattern": "Worldwide Distribution- US (nationwide) including MA, MN, NY and Puerto Rico;  Canada, Mexico, Dubai, Australia, Chile, Colombia, Germany, France, England, Spain, Italy, Norway, Hong Kong, Shanghai, New Zealand, South Africa, Singapore, Japan, Thailand and the Caribbean Islands.",
      "state": "FL",
      "product_description": "RENASYS EZ Negative Pressure Wound Therapy (NPWT) System (RENASYS EZ) for patients who would benefit from a suction device particulary as the device may promote wound healing.",
      "report_date": "20141001",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Smith & Nephew, Inc.",
      "recall_number": "Z-2688-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "69137",
      "termination_date": "20150806",
      "recall_initiation_date": "20140813",
      "postal_code": "33716-1130",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}