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All product recalls associated with Coherent Inc Laser Group.
Total Recalls
1000
Past Year
1000
Class I (Serious)
145
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Software problem that may cause the instrument to remain on and emitting laser radiation after the interlock has been activated.
Drug product cross reacts with the Tricyclic Antidepressants (TCA) assay.
The package inserts contain incorrect values for the alternate unit (mol/L) Control Ranges