{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "29401",
      "product_res_number": "Z-0057-04",
      "event_date_initiated": "2002-01-14",
      "event_date_posted": "2003-10-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-10-27",
      "res_event_number": "27190",
      "product_code": "INX",
      "k_numbers": [
        "K942184"
      ],
      "product_description": "Clinitron At Home Air Fluidized Therapy Unit",
      "code_info": "Model 206 (CS), Serial numbers 101671 and 103443 510K: K942184",
      "firm_fei_number": "1045510",
      "recalling_firm": "Hill-Rom Manufacturing, Inc.",
      "address_1": "4349 Corporate Road",
      "city": "Charleston",
      "state": "SC",
      "postal_code": "29405",
      "additional_info_contact": "Mark Lanning\n843-740-8586",
      "reason_for_recall": "Power cord overheating",
      "root_cause_description": "Other",
      "action": "Consignees were notified by letter sent January 14, 2002 warning them of the hazard involved with the defective part. They were informed that  Hill Rom needed to replace the power cord on each unit to correct the possibility of the power cord from overheating, melting or smoking. The maintenance would be performed at the location of each unit (most of which are at their rental facilities located nationwide) by the firm''s servicing representatives. Meanwhile, customers were urged to check the power cord to ensure that it is fully inserted into the wall outlet and the connector on the Clinitron At Home Air Fluidized Therapy Unit. The modification was to be completed by August 31, 2002.",
      "product_quantity": "1703 units",
      "distribution_pattern": "Hill Rom primarily leases these units to home care patients and some are sold nationwide.",
      "openfda": {
        "k_number": [
          "K881705",
          "K843389",
          "K943385",
          "K964223",
          "K911057",
          "K760712",
          "K884529",
          "K810543",
          "K904008",
          "K926402",
          "K931168",
          "K942184",
          "K913654",
          "K880340",
          "K934689",
          "K890523",
          "K842987",
          "K870045",
          "K834344",
          "K884835",
          "K813584",
          "K972176",
          "K920112",
          "K881917",
          "K924973",
          "K924686",
          "K911246",
          "K852036"
        ],
        "device_name": "Bed, Air Fluidized",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.5160",
        "device_class": "2",
        "registration_number": [
          "3014650138",
          "9611484",
          "3005529226",
          "3018070887",
          "1824206",
          "3007420694"
        ],
        "fei_number": [
          "3014650138",
          "3005529226",
          "3018070887",
          "1824206",
          "3007420694",
          "3002807390"
        ]
      }
    }
  ]
}