{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Wayne",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63878",
      "recalling_firm": "Maquet Inc.",
      "address_1": "45 Barbour Pond Drive",
      "address_2": "N/A",
      "postal_code": "07470",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including AR, GA, SC, TX, TN and internationally to France, United Arab Emirates, Australia, Brazil, Canada, Switzerland, China, Germany, Spain, United Kingdom, Italy, Japan, Sweden, Thailand, Turkey, Serbia, and South Africa.",
      "recall_number": "Z-0627-2013",
      "product_description": "Maquet Yuno Extension Table Device  Maquet GmbH & Co. KG  Kehler Strabe 31  Baden-Wuerttemberg  76437 Rastatt,Germany     Used to support the lower extremities immediately before during and after surgery. The extension device is mounted to the YUNO operating table. The product may only be operated by medically trained staff within the OR environment.",
      "product_quantity": "63 devices",
      "reason_for_recall": "There is a potential issue with the screw tension of the extension device 1433.62A1 used with the YUNO table.",
      "recall_initiation_date": "20121102",
      "center_classification_date": "20130103",
      "termination_date": "20130821",
      "report_date": "20130109",
      "code_info": "Class I exempt  Device Listing Number A922956"
    }
  ]
}