VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System — Class II medical device recall Z-1335-2023
Ongoing recall by Maquet Cardiovascular, LLC, reported 2023-04-12, distributed nationwide. Some batches of product were not sterilized to their minimum sterilization specification.
| Recall number | Z-1335-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Cardiovascular, LLC, Wayne, NJ, United States |
| Recall initiated | 2023-03-06 |
| Classified | 2023-04-04 |
| Reported by FDA | 2023-04-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, CN |
| Quantity | 900 units |
| UPC / GTIN / UDI-DI | 00607567701250 |
| Lot numbers | 3000276183, 3000280189 |
| Model numbers | C-VH-3500 |
Product
VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System, Model Number C-VH-3500
Reason for recall
Some batches of product were not sterilized to their minimum sterilization specification.
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-1335-2023. 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.