Reported Oct 15, 2025 · Ongoing
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m
Corneat Vision, Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: CORNEAT VISION, LTD. · 4, Ha-Sheizaf · Ra'Anana · N/A
Is this the product you have?
- CorNeat EverPatch
- REF
1036295Permanent Tissue-Integrating Surgical Matrix5.0 mm x 605 mm x 100 ¿m
- Lot codes and dates
- All Lots/ UDIG16010362950
- Amount recalled
- 630 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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