Contour VL Variable Length Ureteral Stent — Class II medical device recall Z-0757-2021
Ongoing recall by Boston Scientific Corporation, reported 2021-01-06, distributed nationwide. Trace amounts of metallic debris were found on the stent related to the manufacturing process. The debris was
| Recall number | Z-0757-2021 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Boston Scientific Corporation, Marlborough, MA, United States |
| Recall initiated | 2020-11-16 |
| Classified | 2020-12-30 |
| Reported by FDA | 2021-01-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | JP |
| Quantity | 458 units |
| UPC / GTIN / UDI-DI | 08714729058410, 08714729067986, 08714729068020 |
| Lot numbers | 25578577, 25578740, 25583824, 25598812, 25609220, 25614542, 25614545, 25619687, 25640715, 25641771, 25670518, 25686790, 25686791, 25686792, 25713852, 25741763, 25741770, 25753933, 25753937, 25790349, 25790351, 25795704, 25802759, 25809481, 25822104 |
Product
Contour VL Variable Length Ureteral Stent, UPN M0061801550, M0061801560, M0061801570
Reason for recall
Trace amounts of metallic debris were found on the stent related to the manufacturing process. The debris was confirmed to be particles of nickel.
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-0757-2021. 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.