Recall Ledger

Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR recall (Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha)

Medical deviceClass IIOngoing

Summary: Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha is recalling Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR. Reason: Software anomaly in the patient positioning system may result in positional discrepancy.

What is being recalled

Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR

Why

Software anomaly in the patient positioning system may result in positional discrepancy.

How serious is it

Class II is the middle level: using or being exposed to this product may cause temporary or medically reversible health problems, and the chance of serious harm is remote.

Where it was sold

US distribution to states of: TX, Washington DC (states named: District of Columbia, Texas)

How to tell if yours is affected

Serial Number: CRUS01/ UDI: (01)04560333350006(21)CRUS01(11)190920

What to do

Check the model, lot or serial numbers above against your device. If yours is affected, contact the manufacturer or your healthcare provider before you stop using a device you rely on.

Recall facts

Recall numberZ-1430-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedFebruary 6, 2026
ReportedMarch 4, 2026
CompanyHitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Company locationKashiwa, N/A, Japan
Initiated byVoluntary: Firm initiated
Quantity1 unit

More recalls from Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha · all medical device recalls · recalls from February 2026

Official FDA record