Polaris Ultra Ureteral Stent Set 6FX24CM with — Class II medical device recall Z-1740-2020
Ongoing recall by Boston Scientific, reported 2020-04-29, distributed nationwide. An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a
| Recall number | Z-1740-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Boston Scientific, Marlborough, MA, United States |
| Recall initiated | 2020-03-09 |
| Classified | 2020-04-17 |
| Reported by FDA | 2020-04-29 |
| Distributed | Nationwide (US) |
| Countries outside the US | JP |
| Quantity | 19 units |
| Lot numbers | 24749818, 24913418 |
Product
Polaris Ultra Ureteral Stent Set 6FX24CM with .035 Sensor UPN: M006192132080
Reason for recall
An increase in the rate of complaints for difficulty or inability to track over the guidewire, may result in a procedural delay due to the need to exchange the affected device
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-1740-2020. 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.