CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m
Reported: October 15, 2025 Initiated: August 18, 2025 #Z-0039-2026
Product Description
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m
Reason for Recall
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Details
- Recalling Firm
- CORNEAT VISION, LTD.
- Units Affected
- 630 units
- 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.
- Location
- Ra'Anana
Frequently Asked Questions
What product was recalled? ▼
CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m. Recalled by CORNEAT VISION, LTD.. Units affected: 630 units.
Why was this product recalled? ▼
Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 15, 2025. Severity: Moderate. Recall number: Z-0039-2026.
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