Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
HORIBA custom configured fluorescence instrument Recalled by Horiba Instruments Incorporated Due to HORIBA custom configured fluorescence instrument has a laser...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Horiba Instruments Incorporated directly.
Affected Products
HORIBA custom configured fluorescence instrument, modular Fluorolog-QM
Quantity: 4 units
Why Was This Recalled?
HORIBA custom configured fluorescence instrument has a laser safety defect. This custom configuration of the modular Instrument removed the primary light source and the excitation monochromator. A plastic cap was installed to plug the optical port, where a more durable beam stop should have been used. The defect may allow the class 4 laser beam to burn (or transmit) through the plastic cap to exit the protective enclosure.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Horiba Instruments Incorporated
Horiba Instruments Incorporated has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report