# FDA recall Z-2620-2025

> **Stryker Communications** · Class II · device recall initiated 2025-07-15.

## Product

Chromophare Surgical Light System, REF: CH00000001; SLX to Oculan NFC Upgrade Kit, REF: P60034

## Reason for recall

Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.

## Distribution

US Nationwide distribution in the states of TX, IL, NY, UT, OR, AZ, VT, NY, IL, MN.

## Key facts

- **Recall number:** Z-2620-2025
- **Recalling firm:** Stryker Communications
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-15
- **Report date:** 2025-10-01

- **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-2620-2025

## Citation

> AI Analytics. FDA recall Z-2620-2025. Retrieved 2026-09-04 from https://api.ai-analytics.org/recall/Z-2620-2025. Source: US FDA. Licensed CC0.

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