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hitachi, ltd. radiation oncology systems, kashiwanohamedicalHigh PriorityActive

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

Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR was recalled because software anomaly in the patient positioning system may result in positional discrepancy.. If you have this product, stop using it until you verify your lot or model details.

By RecallRadar Editorial Team

Sourced from FDA. Last verified March 15, 2026.

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Key facts

Date announced
March 4, 2026
Source agency
FDA

This recall involves safety concerns. Take action promptly.

✨ Plain-English Summary

Brand Name: Hitachi Proton Beam Therapy REF: PROBEAT-CR was recalled because software anomaly in the patient positioning system may result in positional discrepancy.. If you have this product, stop using it until you verify your lot or model details.

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

What's Being Recalled

Quoted source excerpt from the official notice.

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

Quick Info

Key facts from the official notice, kept in the article flow for easy cross-checking.

Brand
Hitachi, ltd. radiation oncology systems, kashiwanoha
Category
medical
Source agency
FDA
Announced
March 4, 2026
Country
US
Status
Active

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

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

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

What You Should Do

Follow the remedy path from the official notice using the exact model and serial details above.

  1. 1Stop using the affected product until you verify whether your item is impacted.
  2. 2Check the official recall notice and match your model, lot, or serial details.
  3. 3Follow the official instructions for repair, replacement, refund, or disposal.
Open Official Recall Notice

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source
FDA
Announced by source
March 4, 2026
Last reviewed by RecallRadar
March 15, 2026

Frequently Asked Questions

Am I affected by this recall?

Check the affected models section on this page. The official notice currently lists Serial Number: CRUS01/ UDI: (01)04560333350006(21)CRUS01(11)190920.

What is the remedy for this recall?

Follow the official instructions for repair, replacement, refund, or disposal on the hitachi, ltd. radiation oncology systems, kashiwanoha recall page.

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://api.fda.gov/device/enforcement.json?search=recall_number:Z-1430-2026&limit=1

Keep browsing with these internal hubs: hitachi, ltd. radiation oncology systems, kashiwanoha recall hub and Medical recall hub.

Official Resources

Use these primary sources for final eligibility and claim instructions.

View official notice from FDA

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