Recall Ledger

RayCare 2024A SP1. Oncology Information Systems. recall (RAYSEARCH LABORATORIES AB)

Medical deviceClass IIOngoing

Summary: RAYSEARCH LABORATORIES AB is recalling 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.

What is being recalled

RayCare 2024A SP1. Oncology Information Systems.

Why

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.

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

Worldwide - US Nationwide distribution.

How to tell if yours is affected

Software Version 8.0.1.60193, UDI 0735000201083920240906, Expiration Date: 2030-01-24

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-2646-2026
CategoryMedical device
AgencyU.S. Food and Drug Administration (FDA)
SeverityClass II
StatusOngoing
Recall startedMay 20, 2026
ReportedJuly 8, 2026
CompanyRAYSEARCH LABORATORIES AB
Company locationStockholm, N/A, Sweden
Initiated byVoluntary: Firm initiated
Quantity3 units

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Official FDA record