{
  "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": "Hayward",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89212",
      "recalling_firm": "Reflexion Medical, Inc.",
      "address_1": "25881 Industrial Blvd",
      "address_2": "N/A",
      "postal_code": "94545-2991",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "U.S. Nationwide distribution in the states of CA and TX",
      "recall_number": "Z-0470-2022",
      "product_description": "RefleXion Medical Radiotherapy System -     System Label: \"*** refleXion REF RXM1000 ***\"    Physics Guide/Treatment Delivery User Manual/Treatment Planning User Manual: \"RefleXion X1 Model: RXM1000\"",
      "product_quantity": "3 devices",
      "reason_for_recall": "Due to dose discrepancy when delivering a plan to a patient in a Non-HFS (Head First Supine) orientation specifically in Feet First Supine (FFS).",
      "recall_initiation_date": "20211124",
      "center_classification_date": "20220110",
      "termination_date": "20240708",
      "report_date": "20220119",
      "code_info": "Model: RXM1000  Serial Numbers/UDI Codes: X11001 / (01)00860003983805(11)210125(21)X11001 X11002 / (01)00860003983805(11)210324(21)X11002 X11003 / (01)00860003983805(11)210524(21)X11003"
    }
  ]
}