Vasoview 6 Pro — Class II medical device recall Z-0210-2024
Ongoing recall by Maquet Cardiovascular, LLC, reported 2023-11-08, distributed in AL, AR, CA, FL, GA, IN, KY, MI…. Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different device.
| Recall number | Z-0210-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Cardiovascular, LLC, Wayne, NJ, United States |
| Recall initiated | 2023-09-19 |
| Classified | 2023-11-02 |
| Reported by FDA | 2023-11-08 |
| Distributed | AL, AR, CA, FL, GA, IN, KY, MI, NJ, OK, PA, TN, TX |
| Countries outside the US | CA |
| UPC / GTIN / UDI-DI | 00607567700239 |
| Lot numbers | 3000313857 |
| Model numbers | VH-2400 |
Product
Vasoview 6 Pro (VV6) - Endoscopic Vessel Harvesting System, Model VH-2400 printed on outer label, inner label and IFU, outer box artwork for Vasoview Hemopro 2 (HP2).
Reason for recall
Device packaged inside an incorrect outer box; displaying artwork & illustrations for a different 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-0210-2024. 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.