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

Recall Z-2316-2013 — Advanta SST Grafts <6mm Intended for use in arterial vascular reconstruction, segmental bypass, and for arteriovenous vascular access.

U.S. FDA — Device Enforcement · United States · 2013-07-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2316-2013
Date of alert
2013-07-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Atrium Medical Corporation
Product category
device
Product type
Devices
Reported risk: Inner tray label may adhere to wall of outer tray which make it difficult to remove the tray onto the sterile field
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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