FDA recall, , Moderate risk
Medic Apheresis Platelets, Leukocytes Reduced, Irradiated
Apheresis Platelets, Leukocytes Reduced, Irradiated did not meet platelet yield specifications.
Recall ended Jun 23, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Medic Inc recalled Apheresis Platelets, Leukocytes Reduced, Irradiated because platelet yield did not meet specifications. The recall began March 9, 2025, and was classified by the FDA on June 23, 2026. The product was distributed in Tennessee.
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.
Apheresis Platelets, Leukocytes Reduced, Irradiated
Recall details
- Company began the recall
- Sold in
- Company
- Medic Inc
- Hazard
- Quality testing 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
- 99012
- Recall number
- B-0080-2026
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
Archived
