{
  "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": "Cleveland",
      "address_1": "595 Miner Rd",
      "reason_for_recall": "There's a potential for liquid penetration into the back side of the front control panel of the X-ray diagnostic table, which can cause a short circuit of the terminals of the tilt operation and cause an unintentional tilt of the table.",
      "address_2": "",
      "product_quantity": "41",
      "code_info": "System Serial Numbers:    0162R15403  0162A66105  0162A65401  218134  217530  209677  716334  217721  0162R16001  0162A65301  0162R15803  0162R16002  209669  0162R15504  0162R15602  0162A66104  0162R16007  0162R15802  0162R15702  0162R16003  212866  218047  0162A66005  0162R15603  0162R16004  218085  0162R15804  217296  0162A65402  0162P21004",
      "center_classification_date": "20170111",
      "distribution_pattern": "US Nationwide distribution in the following states: AL, CA, FL, GA, HI, IL, IN, KS, LA, MA, MI, MS, NJ, NY, OH, PA, SC, VA, WI, WV, & WY.",
      "state": "OH",
      "product_description": "FV-RF (Clinix RF Plus)    Product Usage:  A Stationary X-ray System, a device intended for radiographic/fluoroscopic examinations of various anatomical regions. This device may include signal analysis and display equipment, patient and equipment supports, components and accessories.",
      "report_date": "20170118",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems (Cleveland) Inc",
      "recall_number": "Z-1005-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "75994",
      "termination_date": "20180702",
      "more_code_info": "",
      "recall_initiation_date": "20161118",
      "postal_code": "44143-2131",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}