{
  "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": "2026-08-27",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "26761",
      "product_res_number": "Z-0783-03",
      "event_date_initiated": "2003-04-14",
      "event_date_posted": "2003-04-25",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-06-24",
      "res_event_number": "25951",
      "product_code": "KMI",
      "k_numbers": [
        "K021366"
      ],
      "product_description": "MAC-LAB 1000EX systems",
      "code_info": "The affected systems have serial numbers with XC and 4A as 3rd and 4th characters in the serial number",
      "firm_fei_number": "2124823",
      "recalling_firm": "General Electric Medical Systems Information Technology",
      "address_1": "8200 W. Tower",
      "city": "Milwaukee",
      "state": "WI",
      "postal_code": "53223",
      "reason_for_recall": "There is an incorrect jumper set-up on a motherboard of the devices that could eventually cause a polyfuse to overheat resulting in smoke.",
      "root_cause_description": "Other",
      "action": "A letter was sent to the consignees on April 14, 2003 and requested that the consignees correct the device  or contact the firm to have them perform the correction.",
      "distribution_pattern": "The recalled products were shipped to hospitals located nationwide in the United States and to other consignees located worldwide.",
      "openfda": {
        "k_number": [
          "K872358",
          "K934344",
          "K090138",
          "K101109",
          "K924433",
          "K942770",
          "K840295",
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          "K883390",
          "K823926",
          "K943481",
          "K841671",
          "K920206",
          "K911079"
        ],
        "device_name": "Monitor, Bed Patient",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.2400",
        "device_class": "1",
        "registration_number": [
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