SL3 SOFT-TISSUE Laser — Class II medical device recall Z-1186-2013
Terminated recall by Discus Dental LLC, reported 2013-05-08, distributed nationwide. The firm is initiating this recall of the SL3 Soft Tissue Laser equipped with a fiber optic Unifiber system wh
| Recall number | Z-1186-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Discus Dental LLC, Culver City, CA, United States |
| Recall initiated | 2011-07-21 |
| Classified | 2013-04-29 |
| Reported by FDA | 2013-05-08 |
| Terminated | 2013-04-29 |
| Distributed | Nationwide (US) |
| Quantity | 150 units |
| Reason classes | foreign material |
| Model numbers | LR2002 |
Product
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
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1186-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.