{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Cleveland",
      "address_1": "595 Miner Rd",
      "reason_for_recall": "The firm was informed that while raising the patient couch on the system to perform an exam, the couch unexpectedly descended to the lowest point without being commanded to do so.",
      "address_2": "",
      "product_quantity": "153 units total",
      "code_info": "MX8000 Dual v. EXP: System Code #, 728130, Serial #, 8107, 8128, 8152, 8157, 8171, 8212, 8236, 8245, 8263, 8320 & 8357.",
      "center_classification_date": "20150522",
      "distribution_pattern": "Distributed in China.",
      "state": "OH",
      "product_description": "MX8000 Dualv. EXP, 728130.    Computed Tomography X-ray systems intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.",
      "report_date": "20150603",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Medical Systems (Cleveland) Inc",
      "recall_number": "Z-1647-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71177",
      "termination_date": "20170222",
      "more_code_info": "",
      "recall_initiation_date": "20150316",
      "postal_code": "44143-2131",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}