HIGHFDA DEVICE

RayCare 2024A SP1. Oncology Information Systems.

Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.

RAYSEARCH LABORATORIES ABHealth & Personal CareMedical DevicesSoftware Version 8.0.1.60193UDI 0735000201083920240906Expiration Date: 2030-01-24

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
May 20, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
May 20, 2026
Hazard Level
HIGH
Brand
RAYSEARCH LABORATORIES AB
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
RAYSEARCH LABORATORIES AB
Model numbers
Software Version 8.0.1.60193, UDI 0735000201083920240906, Expiration Date: 2030-01-24
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    May 20, 2026

  2. Reported by FDA DEVICE

    July 8, 2026

  3. RecallRadar source check

    July 14, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact RAYSEARCH LABORATORIES AB or your healthcare provider for instructions. Notification method: N/A

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Full Description

RayCare 2024A SP1. Oncology Information Systems.. Reason: Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.. Classification: Class II. Quantity: 3 units. Distribution: Worldwide - US Nationwide distribution.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Software Version 8.0.1.60193
UDI 0735000201083920240906
Expiration Date: 2030-01-24
Affected States
ALL
Report Date
July 8, 2026
Recall Status
ACTIVE

Related Recalls

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Beam set delivery note issues in which there is potential data loss if the beam set delivery note is modified simultaneously and/or if a note is updated during a treatment session, the user is not notified of the change.

RAYSEARCH LABORATORIES AB
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