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U.S. Department of Health and Human Services

Class 2 Device Recall SL3 SOFTTISSUE Laser

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 Class 2 Device Recall SL3 SOFTTISSUE Lasersee related information
Date Initiated by FirmJuly 21, 2011
Date PostedApril 29, 2013
Recall Status1 Terminated 3 on April 29, 2013
Recall NumberZ-1186-2013
Recall Event ID 64621
510(K)NumberK102639 
Product Classification Powered laser surgical instrument - Product Code GEX
ProductSL3 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
Code Information Model LR2002
Recalling Firm/
Manufacturer		 Discus Dental LLC
8550 Higuera St
Culver City CA 90232-2522
For Additional Information Contact
310-845-8200
Manufacturer 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.
FDA Determined
Cause 2		Device Design
ActionDISCUS Dental, sent an "URGENT MEDICAL DEVICE NOTIFICATION" letter dated July 21, 2011. The letter described the product, problem and action to be taken. Customers were instructed tocontact Discus Dental at 1-888-427-9279 for a no-cost replacement. For questions regarding this recall call 310-845-8200.
Quantity in Commerce150 units
DistributionNationwide 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.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = GEX
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