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Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR

Class II
Recalling firm
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Reason for recall
Software anomaly in the patient positioning system may result in positional discrepancy.
Affected products (lot / model / serial)
Serial number: PTFR-01/ UDI:(01)04560333350204(11)240112(21)PTFR-01
Units affected
1
Distribution pattern
US distribution to states of: TX, Washington DC
Firm location
Kashiwa, N/A, Japan
Recall type
Voluntary: Firm initiated
How the firm notified customers
Visit
Product type
Devices
Status
Ongoing
Recall number
Z-1429-2026
Recall initiated
February 6, 2026
FDA classification date
February 20, 2026
FDA report date
March 4, 2026
FDA event ID
98330
Last updated on HTM Vibe
July 24, 2026
View on openFDA