FDA Recall Open, Classified

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

Recall: Z-1430-2026 · Initiated February 6, 2026

Recall

Recall Number
Z-1430-2026
Event Number
98330
Firm
Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha 44-141-1, W 226 Wakashiba Kashiwa Japan
FEI Number
1000162206
Product Code
LHN
Status
Open, Classified
Root Cause
Software design
Initiated
February 6, 2026
Posted
February 20, 2026

Description

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

Reason

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

Action

Between the dates of February 5-11, 2026, Hitachi, Ltd, issued an "URGENT: MEDICAL DEVICE RECALL" notification dated January 21, 2026, via Service Team Manager to affected consignees. Hitachi is asking consignees to take the following actions: 1. Until the PPS software has been updated with the corrected version, users are instructed to follow the System Operation instruction in the document. 2. Users are also asked to post the document in a prominent space and sign its cover. 3. Complete and return the acknowledgment and receipt form. Action by the firm: Hitachi plans to update the PPS software to a corrected version that prevents the mismatch between the commanded error correction parameter and the internal variable. starting in late March 2026 and the users will be contacted after the update. If you have any questions, please call QA Manager at Tel: (408) 986-6300. Monday through Friday, 8:00 AM to 5:00 PM, Central Time.

Distribution

US distribution to states of: TX, Washington DC

Quantity

1 unit