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

Recall Z-0039-2026 — CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m

U.S. FDA — Device Enforcement · Israel · 2025-08-18 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0039-2026
Date of alert
2025-08-18
Country / jurisdiction
Israel
Risk level
Class II
Risk type
recall
Brand
CORNEAT VISION, LTD.
Product category
device
Product type
Devices
Reported risk: Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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