# FDA recall Z-0488-2025

> **Enchroma Inc** · Class II · device recall initiated 2024-09-06.

## Product

EnChroma Safety Glasses with Rx Indoor Universal Lenses:  Martinez Cx1 Indoor Rx, SKU: Cx.PC.IN.MTZ.BK.Rx;  Summit Indoor Rx, Cx.PC.IN.SUM.BK.Rx;  Martinez Black Cx Rx, Cx-3.PC.PT.MTZ.BK.Rx

## Reason for recall

Safety glasses with Rx indoor universal lenses fail to meet high impact safety specifications, which may not provide adequate protection against impact, posing a risk of eye injury.

## Distribution

Worldwide distribution: US (nationwide): IL, OH, NC, IA, AL, SC, NJ, TX, CO, PA, FL, MI, NY, DU, NM, CA, NH, MT, WV, KY, OR, MA, WI, VA, AZ and OUS (foreign): United Arab Emirates, Japan, and Canada.

## Key facts

- **Recall number:** Z-0488-2025
- **Recalling firm:** Enchroma Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-09-06
- **Report date:** 2024-11-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Berkeley, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0488-2025

## Citation

> AI Analytics. FDA recall Z-0488-2025. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0488-2025. Source: US FDA. Licensed CC0.

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