Horiba Instruments Incorporated recalls HORIBA custom configured fluorescence instrument, modular Fluorolog-QM
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…
Read the official notice →- Date
- 2024-07-10
- Country
- United States
- Brand
- Horiba Instruments Incorporated
- Product
- HORIBA custom configured fluorescence instrument, modular Fluorolog-QM
- Classification
- Class II
- Units
- US Nationwide and Worldwide Distribution
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
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- Check the product name, strength and lot number against the official notice.
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- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
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