Class II
Medical Device Recall: Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha · February 6, 2026
Reason for Recall
Software anomaly in the patient positioning system may result in positional discrepancy.
Distribution
US distribution to states of: TX, Washington DC
States Affected
DC, TX
Quantity Affected
1
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1429-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.