Maquet VH-3010 Power Supply — Class II medical device recall Z-1577-2025
Ongoing recall by Maquet Cardiovascular, LLC, reported 2025-04-23, distributed nationwide. Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adeq
| Recall number | Z-1577-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Cardiovascular, LLC, Wayne, NJ, United States |
| Recall initiated | 2025-03-10 |
| Classified | 2025-04-16 |
| Reported by FDA | 2025-04-23 |
| Distributed | Nationwide (US) |
| Countries outside the US | CN, GB, JP, NL, NZ, SG |
| Quantity | 110 units |
| Serial numbers | H23060082G, H24080001G, H24080002G, H24080003G, H24080004G, H24080005G, H24080006G, H24080007G, H24080008G, H24080009G, H24080010G, H24080011G, H24080012G, H24080013G, H24080014G, H24080015G, H24080016G, H24080017G, H24080018G, H24080019G, H24080020G, H24080021G, H24080022G, H24080023G, H24080024G and 85 more |
| Model numbers | VH-3010 |
Product
Maquet VH-3010 Power Supply. Used to deliver power to the harvesting tool of the Vasoview Hemopro EVH System (HemoPro 2).
Reason for recall
Incorrect resistor utilized in the VH-3010 Power Supply, which may cause the jaws of the HemoPro 2 to not adequately heat up.
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-1577-2025. 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.