Recall archive / FDA device enforcement
Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W . — FDA record Z-0723-2024
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Dec 1, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3000-W .
- Reason
- Risk of polyimide particulate matter being present on the endoscopic harvesting vessel system. This issue may result in polyimide particulate matter being introduced into the arterial conduit for patients undergoing a coronary artery bypass graft (CABG) or peripheral bypass graft surgery.
- Classification
- Class II
- Recalling firm
- Maquet Cardiovascular, LLC
- Quantity
- 554 units (OUS)
- Agency-reported status
- Ongoing
- Source record identifier
- Z-0723-2024
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI-DI: 00607567700413, Lots: 3000283735, 3000293031, 3000310304, 3000333956. |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US: OUS: China, Brazil, Hong Kong.
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Jan 24, 2024
- Recall initiation date
- Dec 1, 2023
- Center classification date
- Jan 12, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.