FDA recall, , Moderate risk
West TN Regional Blood Center Apheresis Platelets
Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced were not tested for pH and were distributed.
Recall ended Sep 24, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
The FDA announced that West TN Regional Blood Center recalled 4 units of Apheresis Platelets, PAS, Leukocytes Reduced, Pathogen Reduced because they were not tested for pH. The recall began on July 31, 2025, and was added to the FDA's Enforcement Report on September 24, 2026.
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, PAS, Leukocytes Reduced, Pathogen Reduced
- Affected units
- W040825600465 (double collection); W040825600469 (double collection)
Recall details
- Company began the recall
- Sold in
- Company
- West TN Regional Blood Center
- 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
- 99095
- Recall number
- B-0211-2026
- Quantity recalled
- 4 units
All recalls from West TN Regional Blood Center
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
