{
  "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": "Malvern",
      "address_1": "51 Valley Stream Pkwy",
      "reason_for_recall": "The firm became aware of a potential issue with Artis zee systems bearing model numbers 10094135, 10094137, and 10094141 equipped with a card collimator from a specific lot where a dislocation of the scatter radiation filter inside the card collimator may occur.",
      "address_2": "",
      "product_quantity": "17",
      "code_info": "model numbers 10094135, 10094137, and 10094141 equipped with a card collimator from a specific lot",
      "center_classification_date": "20131114",
      "distribution_pattern": "US Distribution including the states of AZ, KY, PA, IA WV, FL, MO, OK, CA, AR, MT, NY, KS, and CT.",
      "state": "PA",
      "product_description": "Artis zee systems    x-ray, angiographic system",
      "report_date": "20131120",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-0172-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65795",
      "termination_date": "20141029",
      "more_code_info": "",
      "recall_initiation_date": "20130121",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}