{
  "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": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "The potential exists for system movement to be permanently blocked by an activation of the collision sensor integrated in the cover of the collimator even when no collision has occurred.",
      "address_2": "",
      "product_quantity": "6",
      "code_info": "Serial Numbers 164231, 164234, 164240, 164241, 164242, 164244",
      "center_classification_date": "20200113",
      "distribution_pattern": "US Nationwide distribution in the states of FL, IL, IN, MA, PA, VA.",
      "state": "PA",
      "product_description": "Siemens ARTIS pheno, Model # 10849000.  Interventional Fluoroscopic X-Ray System - Product Usage: Angiography system for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients.",
      "report_date": "20200122",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-0807-2020",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "84648",
      "termination_date": "20200501",
      "more_code_info": "",
      "recall_initiation_date": "20191220",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}