# FDA recall Z-1404-2022

> **Xstrahl Limited** · Class II · device recall initiated 2022-04-27.

## Product

X80 RADiant Photoelectric Therapy System

## Reason for recall

There is a potential compatibility issue with the systems and replacement treatment applicators.

## Distribution

US Distribution FL, CA, KY

## Key facts

- **Recall number:** Z-1404-2022
- **Recalling firm:** Xstrahl Limited
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-04-27
- **Report date:** 2022-07-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Walsall, N/A, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1404-2022

## Citation

> AI Analytics. FDA recall Z-1404-2022. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1404-2022. Source: US FDA. Licensed CC0.

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