{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Orlando",
      "address_1": "6280 Hazeltine National Dr Ste 100",
      "reason_for_recall": "Malfunction of the radiation-warning timer and the 3D-specific interval warning. No 5-minute timer dialogs or beeper will occur until the unit is rebooted.",
      "address_2": "",
      "product_quantity": "1 device",
      "code_info": "Serial # 10841.",
      "center_classification_date": "20160825",
      "distribution_pattern": "US Distribution including Puerto Rico and to the states of :FL, GA, VA,MA. ME, MI, NY, NJ, PA, RI, IL, TX, AZ, CA, NV, UT, and WA.",
      "state": "FL",
      "product_description": "Ziehm Vision R, Mobile C-arm for Mobile Fluoroscopic Imaging",
      "report_date": "20160831",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ziehm Imaging Inc",
      "recall_number": "Z-2642-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74013",
      "termination_date": "20190718",
      "more_code_info": "",
      "recall_initiation_date": "20160415",
      "postal_code": "32822-5114",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}