Corneat Vision recalls

Corneat Vision has 3 recalls on record with the FDA and USDA, the earliest in 2025 and the latest reported on 15 Oct 2025. 3 are still ongoing. 2 were reported in the last 12 months. The most frequent reason is sterility.

Total recalls3since 2025

Last 12 months2reported

Class I00% of total

Ongoing3latest 15 Oct 2025

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 1 2Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why corneat vision is recalled

Sterility267%
Other Reasons133%

Product types

Surgical Instruments267%
Other Medical Devices133%

By year

20253100%

Ongoing corneat vision recalls

3 active

Reported	Class	Recall	Company	Reason	Where
15 Oct 2025Device	CLASS II	EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix recalled	Corneat Vision	Sterility	Nationwide
15 Oct 2025Device	CLASS II	CorNeat EverPatch recalled by Corneat Vision	Corneat Vision	Other	Nationwide
17 Sep 2025Device	CLASS II	CorNeat EverPatch recalled by Corneat Vision	Corneat Vision	Sterility	Nationwide

All corneat vision recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
15 Oct 2025Device	CLASS II	EverPatch+, REF: 1044002, Permanent Scleral Reinforcement Matrix recalled	Corneat Vision	Sterility	Nationwide
15 Oct 2025Device	CLASS II	CorNeat EverPatch recalled by Corneat Vision	Corneat Vision	Other	Nationwide
17 Sep 2025Device	CLASS II	CorNeat EverPatch recalled by Corneat Vision	Corneat Vision	Sterility	Nationwide

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.