# FDA recall Z-2478-2025

> **WASATCH PHOTONICS** · Class II · device recall initiated 2025-08-04.

## Product

Wasatch Photonics 785/830-SR and 785-ER-ILC Raman Spectrometers,   Product Models:  785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC,785-ER-ILC.

## Reason for recall

Two new potential laser safety failure modes have been identified in the product design. Overcurrent of laser diode, and a fail-unsafe mode.  The failure modes have never been found to occur in these models, whether in the field or factory, but could potentially occur under excessive force or extreme, continuous vibration.

## Distribution

U.S.

## Key facts

- **Recall number:** Z-2478-2025
- **Recalling firm:** WASATCH PHOTONICS
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-04
- **Report date:** 2025-09-17

- **Voluntary/Mandated:** FDA Mandated
- **Location:** Morrisville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2478-2025

## Citation

> AI Analytics. FDA recall Z-2478-2025. Retrieved 2026-09-07 from https://api.ai-analytics.org/recall/Z-2478-2025. Source: US FDA. Licensed CC0.

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