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

Recall Z-2337-2024 — The VASOVIEW HEMOPRO Endoscopic Vessel Harvesting Systems is designed for use in conjunction with the 7 mm Extended Length Endoscope. The Harvesting Cannula has four lumens which house the Endoscope, C-Ring, distal lens washer tube, and harvesting tool for cutting and cauterizing vessel branches.

U.S. FDA — Device Enforcement · United States · 2024-05-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2337-2024
Date of alert
2024-05-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Maquet Cardiovascular, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00607567700345
Reported risk: There were 27 complaints between March 22, 2024, and April 30, 2024, related to VH-3500 and VH-4000, reporting that the C-Ring wire was straightened (due to insufficient bend radius) and that the distance between C-Ring and Harvesting Tool was closer than normal. No adverse events have been reported to date in direct association with this issue.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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