FDA recall, , Moderate risk
The Blood Connection Apheresis Platelets, Leukocytes Reduced
Apheresis Platelets, Leukocytes Reduced were not tested to verify white blood cell count.
Recall ended Jun 30, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
The Blood Connection, Inc. recalled Apheresis Platelets, Leukocytes Reduced on November 19, 2024, because the platelets were labeled as leukocytes reduced but were not tested to verify white blood cell count. The recall was added to the FDA's Enforcement Report on June 30, 2026, and distributed in New Hampshire.
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
Recall details
- Company began the recall
- Sold in
- Company
- The Blood Connection, 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
- 99243
- Recall number
- B-0145-2026
All recalls from The Blood Connection, Inc.
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
