FDA recall, , Moderate risk
Precision Ocular Network Cornea
Corneas were distributed without adequate donor eligibility determination.
Recall ended Sep 21, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Precision Ocular Network - Bartlett distributed corneas recovered from a donor for whom donor eligibility was not adequately determined. The FDA reported the recall began on August 15, 2024, and was added to its Enforcement Report on September 21, 2026. The corneas were distributed in Alabama and Louisiana.
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
- Company
- Precision Ocular Network - Bartlett
- 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
- 99915
- Recall number
- B-0249-2026
All recalls from Precision Ocular Network - Bartlett
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
