Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CorNeat EverPatch Recalled by CORNEAT VISION, LTD. Due to Reviewed complaints have identified that conjunctival wound dehiscence...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact CORNEAT VISION, LTD. directly.
Affected Products
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m
Quantity: 630 units
Why Was This Recalled?
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CORNEAT VISION, LTD.
CORNEAT VISION, LTD. has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report