{
  "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,
      "total": 1
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  "results": [
    {
      "cfres_id": "26078",
      "product_res_number": "Z-0424-03",
      "event_date_initiated": "2002-11-12",
      "event_date_posted": "2003-03-05",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-02-28",
      "res_event_number": "25571",
      "product_code": "KPR--",
      "product_description": "X-Cel MB-700 A/C Podiatry X-Ray System; X-Cel X-Ray Coporation, 4220 Waller Drive, Crystal Lake, IL 60012",
      "code_info": "Model MB-700 A/C, srial numbers 622686, 622687, 622688, 622689, 320367, 325120",
      "firm_fei_number": "1418484",
      "recalling_firm": "X-Cel X-Ray Corp",
      "address_1": "4220 Waller Drive",
      "city": "Crystal Lake",
      "state": "IL",
      "postal_code": "60012-2848",
      "additional_info_contact": "Mr. William W. Morris\n815-455-2470",
      "reason_for_recall": "The X-Ray system contained a defective X-Ray tube shield.",
      "root_cause_description": "Other",
      "action": "Recalled by telephone call on 11/19/2002, with follow-up visits and letters dated 2/27/03.  The tube shields were replaced and the x-ray units were recertified.",
      "product_quantity": "3 units",
      "distribution_pattern": "Northbrook, IL and Frankfort, IL",
      "openfda": {}
    }
  ]
}