# FDA recall Z-2646-2026

> **RAYSEARCH LABORATORIES AB** · Class II · device recall initiated 2026-05-20.

## Product

RayCare 2024A SP1. Oncology Information Systems.

## 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.

## Key facts

- **Recall number:** Z-2646-2026
- **Recalling firm:** RAYSEARCH LABORATORIES AB
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-05-20
- **Report date:** 2026-07-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Stockholm, N/A, Sweden

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2646-2026

## Citation

> MORVS. FDA recall Z-2646-2026. Retrieved 2026-10-23 from https://api.morvs.ai/recall/Z-2646-2026. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*