{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "32342",
      "product_res_number": "Z-0887-04",
      "event_date_initiated": "2004-03-22",
      "event_date_posted": "2004-07-20",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-11-02",
      "res_event_number": "28683",
      "product_code": "IKZ",
      "product_description": "KCI TriaDyne Proventa Critial Care Therapy System, manufactured by Kinetic Concepts, Inc., San Antonio, Texas 78219.  Model number 308900",
      "code_info": "The following serial numbers: TDBK00029, TDBK00294, TDBK00015, TDBK00291, TDBK00026, TDBK00027, TDBK00123, TDBK00124, TDBK00125, TDBK00127, TDBK00128, TDBK00130, TDBK00132, TDBK00136",
      "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": "Battery outgassing of powered hospital beds",
      "root_cause_description": "Other",
      "action": "The firm initiated the recall via letter on 03/22/2004.",
      "product_quantity": "14 beds",
      "distribution_pattern": "Product was distributed domestically in the following states: IN, CA, NH, OR, PA, TX, WI, CO, IA, KS, MO, ID, MA, NC, IL, OH, MN, AZ, NE, HI, PR, NC",
      "openfda": {
        "k_number": [
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          "K810220",
          "K972111",
          "K822402",
          "K905390",
          "K933964",
          "K922473",
          "K842604",
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          "K950756",
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          "K972486",
          "K823095",
          "K873047",
          "K834563",
          "K962788",
          "K905113"
        ],
        "device_name": "Bed, Patient Rotation, Powered",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.5225",
        "device_class": "2",
        "registration_number": [
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}