{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "San Antonio",
      "address_1": "12930 IH 10 West",
      "reason_for_recall": "Prevena Incisional Management System Kit/Dressing Connector - the male connector on the tubing is difficult to connect to the female connector on the Prevena canister tubing",
      "address_2": "",
      "product_quantity": "20,850 units total",
      "code_info": "Kit Lot # 2410919",
      "center_classification_date": "20140304",
      "distribution_pattern": "USA Nationwide Distribution",
      "state": "TX",
      "product_description": "PRE2055: Prevena Customizable Dressing 5-Pack    Product Usage:  The Prevena Incision Management System is intended to manage the environment of surgical incisions that continue to drain following sutured or stapled closure by maintaining a closed environment and removing exudates via the application of negative pressure wound therapy.",
      "report_date": "20140312",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "KCI USA, INC.",
      "recall_number": "Z-1140-2014",
      "initial_firm_notification": "Visit",
      "product_type": "Devices",
      "event_id": "67454",
      "termination_date": "20150406",
      "more_code_info": "",
      "recall_initiation_date": "20140130",
      "postal_code": "78249",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}