Vista Brite Tip — Class II medical device recall Z-1330-2025
Ongoing recall by Cordis US Corp, reported 2025-03-19. Catheter manufactured at the incorrect length.
| Recall number | Z-1330-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Cordis US Corp, Miami Lakes, FL, United States |
| Recall initiated | 2025-02-07 |
| Classified | 2025-03-13 |
| Reported by FDA | 2025-03-19 |
| Countries outside the US | JP |
| Quantity | 12 units |
| UPC / GTIN / UDI-DI | 20705032042991 |
| Lot numbers | 18368326 |
| Model numbers | JR3VBT, M7504 |
Product
Vista Brite Tip, Judkins Right 4, REF SM7504, JR3 VBT (Special) 110 cm 6F. Guiding catheter is intended for use for intravascular introduction of interventional/diagnostic devices into the coronary or peripheral vascular systems.
Reason for recall
Catheter manufactured at the incorrect length.
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-1330-2025. 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.