Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet… — Class II medical device recall Z-0466-2014
Terminated recall by Maquet Cardiovascular, LLC, reported 2013-12-18, distributed nationwide. Maquet has received an increase in the number of complaints for "self-activated/remains activated/overheats" f
| Recall number | Z-0466-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Cardiovascular, LLC, Wayne, NJ, United States |
| Recall initiated | 2013-10-30 |
| Classified | 2013-12-06 |
| Reported by FDA | 2013-12-18 |
| Terminated | 2015-04-24 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, CH, CZ, DK, FR, GB, HK, IT, NL, SG |
| Quantity | 12,259 units |
| Reason classes | device malfunction |
| Lot numbers | 25073724, 25076133, 25076371, 25076372, 25076989, 25077051, 25077123, 25077563, 25077643, 25077927, 25078103, 25078104, 25078289, 25078291, 25078463, 25078713, 25078777, 25078931, 25079086, 25079363, 25079449, 25079913, 25079982, 25080264, 25080311, 25080351, 25080418, 25080661, 25080744, 25080938, 25080939, 25081204, 25081460, 25081595, 25081686 |
| Model numbers | VH-3000, VH-3000W |
Product
Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular LLC 45 Barbour Pond Drive Wayne, NJ 07470 Indicated for use in minimally invasive surgery allowing access for vessel harvesting and is primarily indicated for patients undergoing endoscopic surgery for arterial bypass. It is indicated for cutting tissue and controlling bleeding through coagulation, and for patients requiring blunt dissection of tissue including dissection of blood vessels, dissection of blood vessels oft he extremities, dissection of ducts and other structures int he extraperitoneal or subcutaneous extremity and thoracic space. Extremity procedures include tissue dissection/vessel harvesting along the saphenous vein for use in coronary artery bypass grafting and peripheral artery bypass or the radial artery for use in coronary artery bypass grafting. Thorascopic procedures include exposure and dissection of structures external to the parietal pleura including nerves blood vessels and other tissues of the chest wall.
Reason for recall
Maquet has received an increase in the number of complaints for "self-activated/remains activated/overheats" for the Hemopro VH-30000, "Hemopro 1"
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-0466-2014. 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.