VasoView HemoPro Endoscopic Vessel Harvesting System — Class I medical device recall Z-0092-2025
Ongoing recall by Maquet Cardiovascular, LLC, reported 2024-11-06, distributed nationwide. There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.
| Recall number | Z-0092-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Cardiovascular, LLC, Wayne, NJ, United States |
| Recall initiated | 2024-09-20 |
| Classified | 2024-10-25 |
| Reported by FDA | 2024-11-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, CN, HK |
| Quantity | 28,809 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00607567700413, 00607567701250 |
| Lot numbers | 3000333967, 3000339701, 3000340534, 3000341133, 3000341675, 3000342250, 3000342251, 3000343264, 3000343266, 3000344887, 3000345068, 3000346640, 3000351187, 3000351376, 3000351407, 3000351619, 3000351747, 3000351860, 3000352770, 3000354226, 3000354228, 3000355224, 3000355369, 3000355798, 3000356048, 3000357837, 3000360574, 3000360576, 3000360775, 3000361036, 3000361423, 3000361707, 3000362064, 3000362258, 3000362671, 3000362933, 3000363162, 3000363947, 3000364082, 3000364309 and 75 more |
Product
VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500
Reason for recall
There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.
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-0092-2025. 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.