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

Recall Z-1865-2020 — HEMASHIELD PLATINUM Woven Double Velour Vascular Graft-Angled 4 Branch, Product Code: M00202175730AP0 - Product Usage: for use in the replacement or repair of arteries affected with aneurysmal or occlusive disease.

U.S. FDA — Device Enforcement · United States · 2020-04-07 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1865-2020
Date of alert
2020-04-07
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Maquet Cardiovascular, LLC
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
1124104830
Reported risk: Potential small holes at the seam lines of Hemashield branches causing intra-operative bleeding at the seam lines of the branches of Hemashield grafts
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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