{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25985",
      "product_res_number": "Z-0157-03",
      "event_date_initiated": "2002-11-21",
      "event_date_posted": "2003-02-12",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-07-02",
      "res_event_number": "25531",
      "product_code": "90LMA",
      "k_numbers": [
        "K012389"
      ],
      "product_description": "Revolution XR/d Wall Stand, Model Number 2291655, for Revolution XR/d Digital Radiographic Imaging Systems",
      "code_info": "All serial numbers in distribution at the time of the recall.",
      "firm_fei_number": "2126677",
      "recalling_firm": "General Electric Med Systems",
      "address_1": "3000 N Grandview Blvd",
      "city": "Waukesha",
      "state": "WI",
      "postal_code": "53186",
      "reason_for_recall": "The devices do not meet requirements in 21 CFR 1010.2 in that they lack certification labels.",
      "root_cause_description": "Other",
      "action": "Field modification instructions were issued on 11/21/02 to GE field engineers who placed the certification label on the equipment.",
      "product_quantity": "78 devices",
      "distribution_pattern": "The product had been shipped to hospitals located nationwide in the United States.",
      "openfda": {}
    }
  ]
}