Reported Jul 10, 2024 · Ongoing
HORIBA custom configured fluorescence instrument, modular Fluorolog-QM
Horiba Instruments Incorporated
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Horiba Instruments Incorporated · 20 Knightsbridge Rd · Piscataway, NJ · 08854-3913
Is this the product you have?
- HORIBA custom configured fluorescence instrument, modular Fluorolog-QM
- Lot codes and dates
- Modular Fluorolog-QM
- Amount recalled
- 4 units
Where it was sold
- Nationwide
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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