FDA recall, , Moderate risk
We Are Blood Red Blood Cells and Pooled Cryoprecipitated AHF
Red Blood Cells, Leukocytes Reduced, collected from a donor who had permanent make-up applied within three months of donation, were distributed.
Recall ended Jul 20, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
We Are Blood recalled Red Blood Cells, Leukocytes Reduced, collected from a donor who had permanent make-up applied within three months of donation, and Pooled Cryoprecipitated AHF, also collected from a donor with permanent make-up applied within three months, both distributed in Texas. The recall began April 7, 2025, and was added to the FDA's Enforcement Report on July 20, 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?
2 products
Compare these details with yours, then check the recall notice to see which units are recalled.
Red Blood Cells, Leukocytes Reduced
Reason: Red Blood Cells, Leukocytes Reduced, collected from a donor who had permanent make-up applied within three months of donation, were distributed.
Pooled Cryoprecipitated AHF
Reason: Pooled Cryoprecipitated AHF, collected from a donor who had permanent make-up applied within three months of donation, were distributed.
Recall details
- Company began the recall
- Sold in
- Company
- We Are Blood
- 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
- 99271
- Recall numbers
- B-0133-2026 to B-0134-2026
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
