{
  "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": [
    {
      "country": "United States",
      "city": "Cleveland",
      "address_1": "595 Miner Rd",
      "reason_for_recall": "Supplier design change contributed to a thinner plastic which was used as part of the cover on the devices. The thinner plastic cover may crack causing injury to patients, operators, by-standers and service personnel.",
      "address_2": "",
      "product_quantity": "10 units",
      "code_info": "901475, 901476, 901495, 901505, 901509, 901513, 901529, 901532, 901539, 901541",
      "center_classification_date": "20160630",
      "distribution_pattern": "Distributed in China, Denmark, Germany, Hungary, Italy, Philippines, Spain, Sweden, Switzerland, Thailand, and United Kingdom.",
      "state": "OH",
      "product_description": "Ingenuity Flex, model # 728317; Intended to produce cross- sectional  images of the body.",
      "report_date": "20160706",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems (Cleveland) Inc",
      "recall_number": "Z-2113-2016",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "74511",
      "termination_date": "20180702",
      "more_code_info": "",
      "recall_initiation_date": "20160621",
      "postal_code": "44143-2131",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}