{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "37369",
      "product_res_number": "Z-0583-05",
      "event_date_initiated": "2003-06-06",
      "event_date_posted": "2005-03-10",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-04-01",
      "res_event_number": "31207",
      "product_code": "IOQ",
      "k_numbers": [
        "K970468"
      ],
      "product_description": "KinAir MedSurg, flotation therapy, powered hospital bed, manufactured by Kinetic Concepts, Inc., San Antonio, Texas",
      "code_info": "Serial Numbers KASK00001 through KASK01212",
      "firm_fei_number": "1625774",
      "recalling_firm": "Kinetic Concepts, Inc",
      "address_1": "4958 Stout Dr",
      "city": "San Antonio",
      "state": "TX",
      "postal_code": "78219-4334",
      "reason_for_recall": "Weld failure causes side rail welds to turn upside down or break off of the bed.",
      "root_cause_description": "Other",
      "action": "The firm initiated the recall by telephone on 06/06/2003.  The firm has inspected and corrected the beds.",
      "product_quantity": "1181 beds",
      "distribution_pattern": "The beds were distributed nationwide and to Brazil.",
      "openfda": {
        "k_number": [
          "K910851",
          "K970295",
          "K893801",
          "K894723",
          "K914674",
          "K882229",
          "K970636",
          "K883192",
          "K832829",
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          "K882607",
          "K926456",
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          "K922140",
          "K122473",
          "K921768",
          "K875321",
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          "K912855",
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          "K871368",
          "K893708",
          "K905053",
          "K903659",
          "K941610",
          "K881843",
          "K920382",
          "K871614",
          "K925694",
          "K914851",
          "K943433",
          "K964873",
          "K771264",
          "K970363",
          "K840882",
          "K882177",
          "K863047",
          "K970364",
          "K951001",
          "K840881",
          "K840697",
          "K905126",
          "K893614",
          "K880486",
          "K931594",
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          "K901890",
          "K922973",
          "K940662",
          "K894353",
          "K143414",
          "K973624"
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        "fei_number": [
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        "device_name": "Bed, Flotation Therapy, Powered",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.5170",
        "device_class": "2"
      }
    }
  ]
}