{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "34400",
      "product_res_number": "Z-0022-05",
      "event_date_initiated": "2004-08-30",
      "event_date_posted": "2004-10-19",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-04-01",
      "res_event_number": "29703",
      "product_code": "IMK",
      "pma_numbers": [
        "P020033"
      ],
      "product_description": "iBOT 3000 Mobility System, Independence iBOT 3000 Mobility System (Stair-climbing wheelchair), Class III restricted medical device.",
      "code_info": "Catalog No.''s IT000101-IT000148 (inclusive), Vehicle Identification Numbers (''VIN''s):  020404-000347, 020104-000309, 020504-000357, 021203-000308, 020204-000331, 020104-000314, 020104-000318, 021203-000301, 020304-000335, 020104-000310, 020404-000341, 021203-000299, 020204-000330, 020104-000322, 020204-000332, 020404-000350, 020404-000348, 020304-000340, 020404-000346, 020404-000342, 021203-000307, 020204-000333, 020104-000319, 021203-000304, 020404-000352, 020304-000337, 020304-000336, 020504-000356, 020404-000349, 021203-000305, 020604-000360, 020104-000317, 021203-000306, 020504-000358, 020404-000345, 020504-000354, 020304-000334, 020304-000338, 020404-000344, 020404-000351, 020504-000355, 020104-000323, 020104-000324, 021103-000291, 021203-000300, 020304-000339, 020404-000343, 020504-000359, 020604-000363, 020604-000364, 020604-000365, 020604-000366, 020604-000367, 020604-000368, 020604-000362, 021103-000290, 021103-000295, 020104-000315, 020104-000316, 020104-000320, 020104-000311, 020104-000313, 020204-000329, 020504-000353, 020104-000312, 020604-000361, 021003-000280, 020204-000328, 020104-000321, 020204-000326, 021203-000297, 021203-000298, 021203-000303, 020204-000327, 021103-000294, 021103-000286, 021103-000287, 021003-000273, 021103-000282, 021103-000292, 021103-000293, 021003-000276, 021003-000277, 021103-000285, 021103-000289, 020204-000325, 021103-000296, 021003-000278, 021003-000281, 021003-000272, 021003-000279, 021003-000274, 021003-000275, 021103-000283, 021103-000288, 021103-000284, 021203-000302.",
      "firm_fei_number": "3003508375",
      "recalling_firm": "Independence Technology LLC",
      "address_1": "45 Technology Dr",
      "city": "Warren",
      "state": "NJ",
      "postal_code": "07059-5148",
      "additional_info_contact": "Susan Eichler-Huston\n908-412-2262",
      "reason_for_recall": "Rocks and debris can enter into the wheel cluster housing through a damaged wheel cap causing wheel malfunction.",
      "root_cause_description": "Other",
      "action": "All individuals/organizations in possession of a device were notified by telephone beginning on August 30, 2004.  Letters were mailed to all Customers on 8/31/2004 and to all Clinics on 9/1/2004.",
      "product_quantity": "81 chairs",
      "distribution_pattern": "The Independence IBOT 3000 Mobility System was distributed to direct customers in the US, the UK, Ireland, and New Zealand.  Ten of the US Direct customers received their devices via the VA.  One training/demo/assessment device was distributed to the firm''s European support Centre (Ortho Clinical Diagnostics) in France.  Two training/demo/assessment devices were distributed to a J&J representative in Japan.",
      "openfda": {
        "k_number": [
          "K210920",
          "K243442",
          "K172601"
        ],
        "pma_number": [
          "P900050",
          "P020033"
        ],
        "device_name": "Wheelchair, Stair Climbing",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.3890",
        "device_class": "2",
        "registration_number": [
          "3014522447",
          "1220973"
        ],
        "fei_number": [
          "3014522447",
          "1220973"
        ]
      }
    }
  ]
}