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CORNEAT VISION, LTD. recalls CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m
Recalled October 15, 2025 · FDA recall Z-0039-2026 · CORNEAT VISION
Hazard
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch. · FDA Class II
Units
630 units
Sold at
Worldwide - US Nationwide distribution in the states of AZ, CA, CO, CT, DC, DE, FL, GA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MT, NC, NY, OH, PA, SC, TN, TX, UT, VA, WA, WI and the countries of Japan, Israel, Argentina, Hong Kong.
Description
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Product
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m
Manufacturer(s)
CORNEAT VISION, LTD.
Made in
Israel
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →