Data Foundry

Medical device recalls 2024

Vasoview Hemopro Endoscopic Vessel Harvesting System — Class II medical device recall Z-0724-2024

Ongoing recall by Maquet Cardiovascular, LLC, reported 2024-01-24. Risk of polyimide particulate matter being present on the endoscopic harvesting vessel system. This issue may

Recall numberZ-0724-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMaquet Cardiovascular, LLC, Wayne, NJ, United States
Recall initiated2023-12-01
Classified2024-01-12
Reported by FDA2024-01-24
Countries outside the USBR, CN, HK
Quantity38,094 units
Reason classesspecification failure
UPC / GTIN / UDI-DI00607567701250
Lot numbers3000279266, 3000280189, 3000281082, 3000281083, 3000281381, 3000281741, 3000282927, 3000283156, 3000286706, 3000287254, 3000288363, 3000288576, 3000289020, 3000289548, 3000289927, 3000290482, 3000291157, 3000291429, 3000291645, 3000292098, 3000293522, 3000293788, 3000293823, 3000294365, 3000295050, 3000295346, 3000296021, 3000296172, 3000296498, 3000297028, 3000299854, 3000300016, 3000300155, 3000300260, 3000301042, 3000301666, 3000302760, 3000303282, 3000303854, 3000304645 and 60 more
Model numbersVH-3500

Product

Vasoview Hemopro Endoscopic Vessel Harvesting System, model VH-3500.

Reason for recall

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.

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-0724-2024. 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.