CorNeat EverPatch surgical patches (REF: 1036295) may cause eye wounds to reopen after surgery. Affected patients should contact the manufacturer for details.
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
CorNeat EverPatch surgical patches (REF: 1036295) may cause eye wounds to reopen after surgery. Patients should contact the manufacturer for specific guidance.
The surgical patch may separate from the eye wound, causing it to reopen. This could lead to infection or further eye damage if not properly managed.
Patients who received the CorNeat EverPatch surgical patch (REF: 1036295) during eye surgery are affected. Those with recent eye surgery are most at risk.
Check for the product name 'CorNeat EverPatch' with reference number REF: 1036295. The patch has dimensions 5.0 mm x 605 mm x 100 micrometers.
Reach out to CorNeat Vision Ltd. for specific guidance on the patch and next steps.
The recall indicates a risk of eye wound reopening, but the manufacturer recommends contacting them directly for specific guidance.
Check for the product name 'CorNeat EverPatch' with reference number REF: 1036295. The patch has dimensions 5.0 mm x 605 mm x 100 micrometers.
The recall does not specify a stop-use action; patients should contact the manufacturer for specific guidance.
We’ve drafted a message you can send CorNeat to request your refund or repair — edit it as you like.
Subject: Recall Z-0039-2026 — CorNeat CorNeat Hello, I own a CorNeat that is covered by recall Z-0039-2026 from CorNeat. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
