{
  "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": "San Antonio",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "62979",
      "recalling_firm": "KCI USA, Inc.",
      "address_1": "4958 Stout Dr",
      "address_2": "N/A",
      "postal_code": "78219-4334",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide) and the countries of Saudi Arabia, United Kingdom, Singapore, Germany, Switzerland, Kuwait, United Arabian Emirates, and Austria.",
      "recall_number": "Z-2466-2012",
      "product_description": "BariAir Therapy System    The BariAir Therapy System is a risk management treatment system designed for large and / or difficult-to-manage patients. The BariAir Therapy System provides low air-loss pressure management therapy, pulsation, percussion, Turn Assist. flexible patient positioning capabilities and built-in scales for patients weighing 300 Ib* to 850 Ib ([136*-386 kg] including accessories). The BariAir Therapy System is indicated to aid in: \" Patients whose body weight and size pose a significant risk or care management issue to the patient or staff during the performance of routine nursing care. \" Large patients weighing between 300 Ib* and 850 Ib (136*-386 kg) including accessories. \" Large patients who are difficult to turn. \" Preventing and treating pressure ulcers. \" Large patients requiring percussion therapy.",
      "product_quantity": "575",
      "reason_for_recall": "KCI has issued a medical device correction for the BariAir Therapy System Hand Pendent.  The BariAir Therapy System is not designed to allow the patient to place the bed into the patient exit position.  KCI has received complaints indicating that patients used the hand pendent to inadvertently place the BariAir Therapy System into a pseudo-exit position.  In a small number of instances, this allow",
      "recall_initiation_date": "20120917",
      "center_classification_date": "20120927",
      "termination_date": "20130729",
      "report_date": "20121003",
      "code_info": "Multiple Serial Numbers with Model Numbers: 404000,405500, 405500RF",
      "more_code_info": ""
    }
  ]
}