{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Hoffman Estates",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91518",
      "recalling_firm": "Siemens Medical Solutions USA, Inc.",
      "address_1": "2501 Barrington Rd",
      "address_2": "N/A",
      "postal_code": "60192-2061",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Japan, Chile, Australia.",
      "recall_number": "Z-1136-2023",
      "product_description": "SIEMENS Biograph Vision:  a) 450, b) 600, c) 600 Edge",
      "product_quantity": "4 units",
      "reason_for_recall": "This is a potential problem with the locking mechanism that is used to secure the PET gantry in either its scanning or service position.",
      "recall_initiation_date": "20230116",
      "center_classification_date": "20230213",
      "report_date": "20230222",
      "code_info": "a) 450:  UDI/DI 405686923807410106, Material Number 10749669, Serial Number 10106;  b) 600:  UDI/DI 405686922450311120, Material Number 10749670, Serial Number 11120;  UDI/DI 405686922450311116, Material Number 10749670, Serial Number 11116;  c) 600 Edge:  UDI/DI 405686918321311068, Material Number 10749672, Serial Number 11068"
    }
  ]
}