---
title: "Wasatch Photonics 785/830-SR and 785-ER-ILC Raman Spectrometers, Product Mode... — FDA record Z-2478-2025 | Is It on Recall"
description: "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 h"
url: https://isitonrecall.com/recall/fda-device-z-2478-2025-wasatch-photonics-785-830-sr-and-785-er-ilc-raman-spectrometers-product-models-785-sr-ilp-785-sr-ilc/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# Wasatch Photonics 785/830-SR and 785-ER-ILC Raman Spectrometers, Product Models: 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, ... — FDA record Z-2478-2025

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 4, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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**: 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.
- **Classification**: Class II
- **Recalling firm**: WASATCH PHOTONICS
- **Quantity**: 192
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2478-2025

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2478-2025%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | all codes included in the model numbers. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

U.S.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Sep 17, 2025
- **Recall initiation date**: Aug 4, 2025
- **Center classification date**: Sep 11, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2478-2025%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [WASATCH PHOTONICS records](https://isitonrecall.com/brand/wasatch-photonics/)