--- title: "CORNEAT VISION, LTD. Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search CORNEAT VISION, LTD. recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/corneat-vision-ltd/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # CORNEAT VISION, LTD. recall records **3** reported ongoing 3 records in this archive. Latest source date Aug 18, 2025. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Aug 18, 2025 FDA device enforcement ### [CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x 100 ¿m](https://isitonrecall.com/recall/fda-device-z-0039-2026-corneat-everpatch-ref-1036295-permanent-tissue-integrating-surgical-matrix-5-0-mm-x-605-mm-x-100-m/) Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch. Class II Reported ongoing 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 th... [Official source for CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 605 mm x ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0039-2026%22) Aug 18, 2025 FDA device enforcement ### [EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5 mm Shield/1 x 5.0mm x 6.5 mm Rectangle, STERILE VH202](https://isitonrecall.com/recall/fda-device-z-0040-2026-everpatch-ref-1044002-permanent-scleral-reinforcement-matrix-1x5-0mm-x-8-5-mm-shield-1-x-5-0mm-x-6-5/) Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch. Class II Reported ongoing 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 th... [Official source for EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix 1x5.0mm x 8.5 mm Shield/1 x 5.0m...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0040-2026%22) Oct 16, 2024 FDA device enforcement ### [CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 mm x 100 um, SterileEO, RX only](https://isitonrecall.com/recall/fda-device-z-2537-2025-corneat-everpatch-ref-1036295-permanent-tissue-integrating-surgical-matrix-5-0-mm-x-6-5-mm-x-100-um/) Retroactive; Due to complaints, labeling correction for permanent tissue-integrating surgical matrices to include prevention and management of would dehiscence. Class II Reported ongoing Distribution: Worldwide - US Nationwide distribution in the states of AZ, CA, CO, DE, FL, GA, ID, IL, IN, KS, MA, MD, MI, MN, MO, MT, NC, NY, OH, PA, SC, TN, TX, UT, VA, WA, WI, Puerto Rico a... [Official source for CorNeat EverPatch, REF: 1036295, Permanent Tissue-Integrating Surgical Matrix, 5.0 mm x 6.5 mm x ...](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2537-2025%22) ## Reasons in these listed records - Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch. - Retroactive; Due to complaints, labeling correction for permanent tissue-integrating surgical matrices to include prevention and management of would dehiscence. These examples come from this result page and are not a ranking of every recall reason. ## Checking CORNEAT VISION, LTD. ### Is there a recall on corneat vision, ltd. right now? This archive contains 3 records, including 3 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search CORNEAT VISION, LTD.](https://isitonrecall.com/check/?q=CORNEAT%20VISION%2C%20LTD.) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)