{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Palo Alto",
      "address_1": "911 Hansen Way",
      "reason_for_recall": "Varian Medical Systems has received reports that unintended changes were made to planned couch  parameters, specifically the couch rotation parameter, during patient set-up. This can occur when a user  sets a different couch rotation from the plan couch rotation while performing patient alignment with Optical  Surface Monitoring System [OSMS].",
      "address_2": "",
      "product_quantity": "21 AlignRT Plus in US, 1 International.",
      "code_info": "TrueBeam version 2.0/2.5 with any version OSMS.    AlignRT Serial Numbers:  247-0200  247-0209  248-0013  248-0057  248-0070  249-0057  249-0066  249-0163  249-0164  249-0195  249-0226  249-0274  249-0050  249-0286  249-0277  248-0044  249-0227  247-0208  249-0047  247-0218  248-0050  248-0043  248-0048  249-0293  249-0155.",
      "center_classification_date": "20160711",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) and countries of: Austria, Azerbaijan, Brunei Darussalam, Bulgaria, Denmark, Georgia, Germany, India, Italy, Malaysia, Morocco, Norway, Portugal, Switzerland, and United Kingdom.",
      "state": "CA",
      "product_description": "Optical Surface Monitoring System{Align RT Plus} This is used on Varian's TrueBeam EDGE;    Radiology: The AlignRT Plus system is indicated for use to position  and monitor patients relative to the prescribed treatment isocentre, and to Withhold the beam automatically during radiation delivery.",
      "report_date": "20160720",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Varian Medical Systems, Inc.",
      "recall_number": "Z-2150-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74585",
      "termination_date": "20180824",
      "more_code_info": "",
      "recall_initiation_date": "20160623",
      "postal_code": "94304-1028",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}