# FDA recall Z-1275-2018

> **RAYSEARCH LABORATORIES AB** · Class II · device recall initiated 2018-01-26.

## Product

Ray Station 4.9 Ray Station 5, Ray Station 6 and Ray Station 7 Software build numbers: 4.9.0.42, 5.0.0.37, 5.0.1.11, 5.0.2.35, 6.0.0.24, 6.1.0.26, 6.1.1.2, 6.2.0.7 or 7.0.0.19  UDI: 0735000201006820171130

## Reason for recall

Software issue with Center Beam in Field functionality. Issue can result in incorrect treatment volume delivered to patient.

## Distribution

Nationwide

## Key facts

- **Recall number:** Z-1275-2018
- **Recalling firm:** RAYSEARCH LABORATORIES AB
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-01-26
- **Report date:** 2018-04-04
- **Termination date:** 2020-01-13

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1275-2018

## Citation

> AI Analytics. FDA recall Z-1275-2018. Retrieved 2026-06-23 from https://api.ai-analytics.org/recall/Z-1275-2018. Source: US FDA. Licensed CC0.

---

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