Discus Dental LLC: Medical Device Recall in 2013 - (Recall #: Z-1186-2013)
Updated on March 25, 2026.
See the recall detail below. You can also see other recalls from the same firm in 2013.
Data Source: FDA.
Product Description:
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
Product Classification:
Class II
Date Initiated: July 21, 2011
Date Posted: May 8, 2013
Recall Number: Z-1186-2013
Event ID: 64621
Reason for Recall:
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.
Status: Terminated
Product Quantity: 150 units
Code Information:
Model LR2002
Distribution Pattern:
Nationwide Distribution including AL, AZ, CA, CO, FL, GA, IA, ID, IL, IN, KS, MA, MD, MI, MO, MT NH, NJ, NM, NV, NY, OH, PA, SD, TX, UT, VA, and WA.
Voluntary or Mandated:
Voluntary: Firm initiated