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

Recall Z-2263-2020 — Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I, TV-AB2680-J, TV-AB2980-I, TV-AB2980-J, TV-AB3480-I, TV-AB3480-J

U.S. FDA — Device Enforcement · United States · 2020-05-06 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2263-2020
Date of alert
2020-05-06
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
Endologix, Inc.
Product category
device
Product type
Devices
Reported risk: A material weakness adjacent to the polymer fill channel may become compromised during pressurization with liquid polymer. Polymer leaks may occur during implantation of abdominal stent graft system. Clinical events related to polymer leaks may be systemic and/or aneurysm related.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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