Class II

Medical Device Recall: CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m

CORNEAT VISION, LTD. · August 18, 2025

Reason for Recall

Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.

Distribution

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.

States Affected

NATIONWIDE

Quantity Affected

630 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0039-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

CORNEAT VISION, LTD. Medical Device Recall: CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m | SafeCheck