{
  "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": "2026-08-27",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "86538",
      "product_res_number": "Z-0662-2010",
      "event_date_initiated": "2009-11-04",
      "event_date_posted": "2010-01-25",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-01-21",
      "res_event_number": "53802",
      "product_code": "IOQ",
      "product_description": "AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA.  Power Cord #4100079 used with Kinair IV Model 22600, Kinair IV 60601 Model 216050, Triadyne Proventa Model 406000, Therapulse ATP/II Models 227800 and 227080.S, Kinair Medsurg Model 201001W, and Kinair Medsurg Pulse Model 40900.",
      "code_info": "Device serial numbers affected:  Kinair IV: KAPK00523 - KAPK00691;  Kinair IV 60601:  KAUK00001 - KAUK00134;  Triadyne Proventa:  TDDK0001 - TDDK00367;  Therapulse ATP: TPNK00001 - TPNK00177;  Kinair Medsurg:  1440-1441, KAS01524, KASK01004 - KASK02930;  and Kinair Medsurg Pulse:  KATK00001 - KATK00655",
      "firm_fei_number": "1625774",
      "recalling_firm": "KCI USA, Inc.",
      "address_1": "4958 Stout Dr",
      "city": "San Antonio",
      "state": "TX",
      "postal_code": "78219-4334",
      "additional_info_contact": "210-255-5571",
      "reason_for_recall": "Power cords may crack and fail inside plug with potential for fire hazard.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "Kinetics Concepts, Inc. (KCI) issued an \"Urgent Medical Device Correction\"  letter dated November 4, 2009.  Consignees were informed of the affected product and instructed to take necessary action to avoid any further issues associated with the product.  \n\nFor further information, contact KCI's technical support team at 1-800-275-4524 option #3.",
      "product_quantity": "4,637 units",
      "distribution_pattern": "Nationwide and Canada",
      "openfda": {
        "k_number": [
          "K882607",
          "K925694",
          "K945729",
          "K912854",
          "K901295",
          "K864232",
          "K881843",
          "K882229",
          "K922140",
          "K905126",
          "K832829",
          "K771264",
          "K143414",
          "K914674",
          "K920382",
          "K964873",
          "K890935",
          "K951001",
          "K915671",
          "K894723",
          "K122473",
          "K840881",
          "K970364",
          "K875321",
          "K882177",
          "K923977",
          "K912855",
          "K926456",
          "K883192",
          "K880486",
          "K903659",
          "K840882",
          "K921768",
          "K932480",
          "K910851",
          "K914851",
          "K905156",
          "K871614",
          "K840697",
          "K973624",
          "K922973",
          "K970295",
          "K970636",
          "K970363",
          "K871368",
          "K926189",
          "K901890",
          "K893614",
          "K940662",
          "K943433",
          "K941610",
          "K893708",
          "K894353",
          "K863047",
          "K931594",
          "K905053",
          "K893801"
        ],
        "registration_number": [
          "3009591865",
          "3014650138",
          "8043439",
          "2030732",
          "3007420694",
          "3017486514",
          "3031218453",
          "1931307",
          "1834244",
          "1954156",
          "1831750",
          "3008058231",
          "3011489684",
          "2032121",
          "8022290",
          "1824206",
          "3007309299",
          "3003542872",
          "3006697241",
          "3012292104",
          "2030595",
          "3036779619",
          "9710603",
          "3010010434",
          "3007005431"
        ],
        "fei_number": [
          "3009591865",
          "3014650138",
          "1000220700",
          "3007420694",
          "3017486514",
          "3003083675",
          "3031218453",
          "1931307",
          "1831750",
          "3004411059",
          "3008058231",
          "3011489684",
          "3000204953",
          "3003513125",
          "3002693132",
          "1824206",
          "3007309299",
          "3003542872",
          "3000040879",
          "3006697241",
          "3012292104",
          "3036779619",
          "1000518730",
          "3010010434",
          "3007005431"
        ],
        "device_name": "Bed, Flotation Therapy, Powered",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.5170",
        "device_class": "2"
      }
    }
  ]
}