Class II

Medical Device Recall: RayCare 2024A SP4. Oncology Information Systems.

RAYSEARCH LABORATORIES AB · May 20, 2026

Reason for Recall

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

Worldwide - US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

3 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2647-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.