{
  "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": "Orlando",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66976",
      "recalling_firm": "Ziehm Imaging Inc",
      "address_1": "6280 Hazeltine National Dr",
      "address_2": "Suite 100",
      "postal_code": "32822-5114",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA (Nationwide) Distribution including the states of AK, AL, AZ, CA, CO, CT, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MT, MA, MD, MI, MN, MN, MO,MS, NC ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and Hawaii.",
      "recall_number": "Z-0566-2014",
      "product_description": "Ziehm Vision(2) FD C-Arm Interventional Fluoroscopic X-Ray System.    Mobile Fluoroscopic Imaging",
      "product_quantity": "1 device",
      "reason_for_recall": "Engineering change in 2006 resulted in a minor non-conformity of their devices. Specifically the emergency switch was changed from a standard component to just an option on the devices.",
      "recall_initiation_date": "20131121",
      "center_classification_date": "20131224",
      "termination_date": "20140623",
      "report_date": "20140101",
      "code_info": "90842",
      "more_code_info": ""
    }
  ]
}