Drug recall

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

FDA recall event 97520 · Class II · WASATCH PHOTONICS

Key facts

Event ID 97520
Recall numbers Z-2478-2025
Recalling firm WASATCH PHOTONICS
Product type Devices
Products 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.
Classification Class II
Status Ongoing
Voluntary or mandated FDA Requested
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…
Initiation date Aug 4, 2025
Report date Sep 17, 2025
City Morrisville
State NC
Country United States
FEI number 3014813917

At a glance

  • 1–9 Products in this recall
  • None FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA drug and product recalls

FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.

Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

Browse all FDA drug and product recalls