FDA recall, , Low risk
Eversight Illinois Cornea
Corneas, not tested adequately and appropriately to reduce the risk of transmission of relevant communicable diseases, were distributed.
Recall ended Sep 21, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Eversight Illinois began a recall of corneas on January 26, 2024, because the corneas were not tested adequately and appropriately to reduce the risk of transmission of relevant communicable diseases. The recall was added to the FDA's Enforcement Report and classified by the FDA on September 21, 2026, and was in the FDA's weekly enforcement report on September 30, 2026. The distribution was to Egypt.
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
EGYPT
- Company
- Eversight Illinois
- Hazard
- Quality testing problem
- Risk
Low risk
Taking it is unlikely to cause health problems.
FDA Class III recall · How risk is rated
- Event ID
- 99912
- Recall number
- B-0246-2026
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
Added to FDA's Enforcement Report · Classified by FDA · Recall ended
In FDA's weekly enforcement report
Listed on Recall Canary
