{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88962",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution",
      "recall_number": "Z-0297-2022",
      "product_description": "Artis zee ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure\t                  Model Number:10094137",
      "product_quantity": "8 units",
      "reason_for_recall": "If SID (source-to-image distance) lift movement is activated and x-ray shall be released simultaneously; x-ray is not possible and the message No x-ray, try again is displayed, may result in a short delay in procedure",
      "recall_initiation_date": "20211020",
      "center_classification_date": "20211124",
      "termination_date": "20240618",
      "report_date": "20211201",
      "code_info": "Serial Numbers:  Serial  150002  150017  125700  150005  150023  150009  150015  150003  Expanded Recall 11/15/21:  147120  147119  150011",
      "more_code_info": ""
    }
  ]
}