Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SL3 SOFT-TISSUE Laser (Model LR2002) Recalled by Discus Dental LLC Due to The firm is initiating this recall of the...
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 Discus Dental LLC directly.
Affected Products
SL3 SOFT-TISSUE Laser (Model LR2002); Manuf: Discus Dental, LLC, 8550 Higuera Street, Culver City CA 90232. The SL3 is a soft-tissue diode laser intended to be used for dental procedures
Quantity: 150 units
Why Was This Recalled?
The firm is initiating this recall of the SL3 Soft Tissue Laser equipped with a fiber optic Unifiber system which contains a fragile glass filament because the fiber broke near the hand piece.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Discus Dental LLC
Discus Dental LLC 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