FDA recall, , Moderate risk
We Are Blood Pooled Platelets, Leukocytes Reduced, Irradiated
Pooled Platelets, Leukocytes Reduced, Irradiated were not tested for pH.
We Are Blood began this recall on Oct 1, 2025. FDA posted it on Oct 27, 2026, the day the recall ended.
Summary by Recall Canary from the FDA notice
What happened
We Are Blood, based in Austin, Texas, voluntarily recalled Pooled Platelets, Leukocytes Reduced, Irradiated because the product was not tested for pH. The recall began on October 1, 2025, and was classified by the FDA on October 27, 2026, with the product distributed in Texas.
What to do
Biologics such as blood, tissue and vaccines are usually given by hospitals and clinics. If you had a transfusion, transplant, infusion or vaccine, ask the place that treated you whether this product was used. If they contact you, follow their advice.
What was recalled
Hospitals, clinics and blood banks match these details against their records.
Pooled Platelets, Leukocytes Reduced, Irradiated
- Unit number
- W221625850627
Recall details
- Posted by FDA
- Recall began
- Status
- Ended Oct 27, 2026
- Weekly archive
- Listed the week of Oct 26, 2026
- Distributed to
- Recalled by
- We Are BloodAustin, Texas
- Hazard
- Quality testing problem
- Risk
Moderate risk
Its use may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- FDA event number
- 100023
- Recall number
- B-0005-2027
- Recall type
- Voluntary: Firm initiated
- How the company first told customers
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Timeline
FDA's Enforcement Report is its public list of recalls; FDA posts a recall by adding it there.
We Are Blood began the recall
FDA posted the recall to its Enforcement Report, rated it Class II (moderate risk) and closed it
Added to Recall Canary
Summary updated