{
  "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": "Saint Petersburg",
      "address_1": "970 Lake Carillon Dr Ste 110",
      "reason_for_recall": "Lack of 510k clearance for design modification.",
      "address_2": "",
      "product_quantity": "15,960 units in the US",
      "code_info": "Model No. 66800164; All pumps of this model are affected.",
      "center_classification_date": "20170118",
      "distribution_pattern": "Nationwide",
      "state": "FL",
      "product_description": "Smith & Nephew, RENASYS GO Negative Pressure Wound Therapy, Rx only.     Intended for patients who would benefit from a suction device to help promote wound healing by removing fluids, including irrigation and body fluids, wound exudates and infectious materials. Used for chronic, acute, traumatic, subacute, and dehisced wounds/ulcers/partial thickness burns/flaps/grafts.",
      "report_date": "20170125",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Smith & Nephew, Inc.",
      "recall_number": "Z-1041-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75966",
      "more_code_info": "",
      "recall_initiation_date": "20161111",
      "postal_code": "33716-1130",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}