{
  "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-0301-2022",
      "product_description": "Artis Q ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure\t\t          Model Number: 10848281",
      "product_quantity": "67 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:  110088  110059  110103  110035  110046  110005  110058  110056  110062  109523  109645  110067  110095  110051  110001  110020  110007  110093  110069  110075  109627  110042  110043  110048  110061  110063  110064  110032  110047  110102  110039  110040  110023  110065  110052  110018  110072  110081  110036  110054  110053  110044  110031  110016  110037  110077  109497  110079  110099  110027  110049  110066  110024  110017  110025  110100  110083  110091  110006  110055  110026  110022  110000  133501  110057  110104  110041  Expanded Recall 11/15/21:  110096  110014",
      "more_code_info": ""
    }
  ]
}