{
  "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": "During Ziehm Imaging GmbH FDA inspection, the label for the Collimator and X-ray Control panel was missing the manufacturer date as part of the identification for certified component",
      "address_2": "",
      "product_quantity": "US - 2 systems",
      "code_info": "S/N 52199, 52108",
      "center_classification_date": "20170516",
      "distribution_pattern": "US Distribution to the states of : FL and CA.  No devices listed in this recall where distributed any foreign /military/government consignees from the U.S.A.",
      "state": "FL",
      "product_description": "Ziehm Imaging solo FD Mobile Fluoroscopic C-arm",
      "report_date": "20170524",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ziehm Imaging Inc",
      "recall_number": "Z-1893-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77030",
      "termination_date": "20191211",
      "more_code_info": "",
      "recall_initiation_date": "20170223",
      "postal_code": "32822-5114",
      "voluntary_mandated": "FDA Mandated",
      "status": "Terminated"
    }
  ]
}