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Pooled Cryoprecipitated AHF
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DRUG RECALLMODERATE

Pooled Cryoprecipitated AHF

Vitalant recalls Pooled Cryoprecipitated AHF for not meeting specifications.

What to do

Healthcare providers should check their inventory for affected units and discontinue use immediately. Contact Vitalant for further instructions and return or dispose of the product as directed.

Recalled
Listed
Updated
Agency
FDA
Firm
Vitalant
Recall ID
99431
Status
ONGOING

Why it was recalled

Vitalant is recalling Pooled Cryoprecipitated AHF because it was not prepared in accordance with specifications. The affected product was distributed to healthcare facilities.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-09-03 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification