{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "25372",
      "product_res_number": "Z-0718-03",
      "event_date_initiated": "1997-06-01",
      "event_date_posted": "2003-04-10",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-07-08",
      "res_event_number": "25201",
      "product_code": "INX",
      "product_description": "TransportAir, Accessory to an Air Bed, Auxiliary Blower Unit, manufactured by Kinetic Concepts, Inc.",
      "code_info": "Serial numbers 0550037 through 0559399.",
      "firm_fei_number": "1625774",
      "recalling_firm": "Kinetic Concepts, Inc",
      "address_1": "4958 Stout Drive",
      "city": "San Antonio",
      "state": "TX",
      "postal_code": "78219",
      "reason_for_recall": "Battery out-gassing due to battery over charging and/or secondary failure mode of deep-discharge.",
      "root_cause_description": "Other",
      "action": "In approximately November 1997 the firm implemented the TransportAir retrograde for all active units.",
      "product_quantity": "4264",
      "distribution_pattern": "Nationwide",
      "openfda": {
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        "device_name": "Bed, Air Fluidized",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.5160",
        "device_class": "2"
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}