FDA recall, , Moderate risk
Vitalant Pooled Cryoprecipitated AHF
Pooled Cryoprecipitated AHF was not prepared in accordance with specifications.
Recall ended Sep 2, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Vitalant recalled Pooled Cryoprecipitated AHF because the product was not prepared in accordance with specifications. The recall began on April 22, 2026, and was added to the FDA's Enforcement Report on September 2, 2026. The product was distributed in Illinois.
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.
Pooled Cryoprecipitated AHF
Recall details
- Company began the recall
- Sold in
- Company
- Vitalant
- 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
- 99431
- Recall number
- B-0191-2026
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
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
