CorNeat Vision Recalls

3 recalls found for CorNeat Vision. Check if any of your products are affected.

HIGHFDA DEVICE

CorNeat Vision Recalls Surgical Matrix Over High Dehiscence Risk

CorNeat Vision recalled 630 units of the EverPatch surgical matrix on August 18, 2025. The recall follows complaints of conjunctival wound dehiscence leading to potential exposure of the surgical patch. The product was distributed worldwide, including across numerous U.S. states.

CorNeat Vision
Reviewed complaints
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HIGHFDA DEVICE

CORNEAT VISION Recalls EverPatch+ Due to Conjunctival Wound Risk

CORNEAT VISION recalled 180 units of EverPatch+ on August 18, 2025, due to a risk of conjunctival wound dehiscence. This defect may lead to early exposure of the surgical patch. The recall affects distribution across the United States and several countries.

CORNEAT VISION
Reviewed complaints
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HIGHFDA DEVICE

CorNeat Vision Recalls Surgical Matrix Over Labeling Issue

CorNeat Vision recalled the CorNeat EverPatch surgical matrix on October 16, 2024. The recall affects the product's labeling for prevention and management of wound dehiscence. Distribution spans across the U.S. and several countries.

CORNEAT VISION
Retroactive; Due
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Brand Statistics

Total Recalls
3
Pages
1