Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0092-2025 — VasoView HemoPro Endoscopic Vessel Harvesting System, Product Codes VH-3000-W and VH-3500

U.S. FDA — Device Enforcement · United States · 2024-09-20 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0092-2025
Date of alert
2024-09-20
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Maquet Cardiovascular, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00607567700413
Reported risk: There were reports of the silicone detaching from the Jaws of the Harvesting Tool during use.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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