FDA recall, , Moderate risk
Eversight Illinois Cornea
Cornea was processed without the proper antibiotic soak.
Recall ended Sep 21, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Eversight Illinois recalled cornea processed without conducting the proper antibiotic soak. The recall began March 1, 2024, and the FDA added it to the Enforcement Report on September 21, 2026. The cornea was distributed in Pakistan.
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
PAKISTAN
- Company
- Eversight Illinois
- Hazard
- Processing problem
- 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
- 95801
- Recall number
- B-0247-2026
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