StarMedTec LightTrail¿ Reusable Fibers — Class II medical device recall Z-0049-2015
Terminated recall by Boston Scientific Corporation, reported 2014-10-15, distributed in NY, TX. Product is not cleared for use with lasers other than the Auriga XL system
| Recall number | Z-0049-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Boston Scientific Corporation, Marlborough, MA, United States |
| Recall initiated | 2014-09-30 |
| Classified | 2014-10-08 |
| Reported by FDA | 2014-10-15 |
| Terminated | 2014-11-26 |
| Distributed | NY, TX |
| Quantity | 5 units |
| Reason classes | unapproved product |
| Lot numbers | 2011-00238 |
| Model numbers | 6453 |
Product
StarMedTec LightTrail¿ Reusable Fibers, 365 um; Material/Part Number: 6453
Reason for recall
Product is not cleared for use with lasers other than the Auriga XL system
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-0049-2015. 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.