FDAClass IIMarch 4, 2026

Brand Name: Hitachi Proton Beam Therapy System recall: Software Issue

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

Why was Brand Name: Hitachi Proton Beam Therapy System recalled?

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

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial number: PTFR-01/ UDI:(01)04560333350204(11)240112(21)PTFR-01

Product
Brand Name: Hitachi Proton Beam Therapy System Ref: PROBEAT-FR
Recalling firm
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Quantity
1
Distribution
US distribution to states of: TX, Washington DC
Recall date
March 4, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls