# FDA recall Z-0040-2026

> **CORNEAT VISION, LTD.** · Class II · device recall initiated 2025-08-18.

## Product

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

## Reason for recall

Reviewed complaints have identified that conjunctival wound dehiscence may result in early exposure of the surgical patch.

## 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.

## Key facts

- **Recall number:** Z-0040-2026
- **Recalling firm:** CORNEAT VISION, LTD.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-18
- **Report date:** 2025-10-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Ra'Anana, Israel

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0040-2026

## Citation

> AI Analytics. FDA recall Z-0040-2026. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-0040-2026. Source: US FDA. Licensed CC0.

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