FDA recall, , Moderate risk
Eversight Illinois Cornea
Corneas were distributed when donor eligibility was not adequately determined.
Recall ended Sep 30, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Eversight Illinois recalled corneas that were distributed from a donor whose eligibility was not adequately determined. The recall began on December 17, 2025, and was classified by the FDA on September 30, 2026. The FDA added the recall to its Enforcement Report on October 1, 2026, and it was included in the weekly enforcement report on October 7, 2026. The recall involved corneas distributed in Illinois.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is yours affected?
Compare these details with yours, then check the recall notice to see which units are recalled.
Cornea
Recall details
- Company began the recall
- Sold in
- Company
- Eversight Illinois
- Hazard
- Blood donor screening
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 100006
- Recall number
- B-0281-2026
All recalls from Eversight Illinois
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Classified by FDA · Recall ended
Added to FDA's Enforcement Report
In FDA's weekly enforcement report
Listed on Recall Canary
