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
Reported: October 15, 2025 Initiated: August 18, 2025 #Z-0040-2026
Product Description
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.
Details
- Recalling Firm
- CORNEAT VISION, LTD.
- Units Affected
- 180 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? ▼
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. Recalled by CORNEAT VISION, LTD.. Units affected: 180 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-0040-2026.
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