FDA recall record

RAYSEARCH LABORATORIES AB RayCare 2024A SP1. Oncology Information Systems recall — FDA Z-2646-2026

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…

Class IIclassification
Z-2646-2026official record ID
Jul 8, 2026report date

Recall record at a glance

Official recordZ-2646-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmRAYSEARCH LABORATORIES AB
Report dateJul 8, 2026
Recall initiation dateMay 20, 2026
Quantity3 units
LocationStockholm, N/A, Sweden

Official product description

RayCare 2024A SP1. Oncology Information Systems.

Why the product was recalled

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.

Distribution information

Worldwide - US Nationwide distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: N/A.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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