# FDA recall Z-1506-2024

> **Stryker Communications** · Class II · device recall initiated 2024-02-08.

## Product

Chromophare Surgical Light System , REF CH00000001

## Reason for recall

Due to insufficient mounting force the stability of surgical light system cannot be guaranteed.

## Distribution

US: None OUS: Chili

## Key facts

- **Recall number:** Z-1506-2024
- **Recalling firm:** Stryker Communications
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-08
- **Report date:** 2024-04-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Flower Mound, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1506-2024

## Citation

> AI Analytics. FDA recall Z-1506-2024. Retrieved 2026-06-30 from https://api.ai-analytics.org/recall/Z-1506-2024. Source: US FDA. Licensed CC0.

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