FDA recall, , Moderate risk
Eversight Illinois Cornea
Cornea, recovered from a donor whose donor eligibility determination failed to ensure that the donor was free from risk factors for, and clinical evidence of infection due to relevant communicable disease agents and diseases, was distributed.
Recall ended Sep 30, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Eversight Illinois is recalling Cornea, recovered from a donor whose donor eligibility determination failed to ensure that the donor was free from risk factors for, and clinical evidence of infection due to relevant communicable disease agents and diseases, was distributed. The recall began on January 15, 2026, and was classified by the FDA on September 30, 2026. The product was distributed in Michigan.
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
- 100008
- Recall number
- B-0283-2026
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
