Drug recall

Pooled Cryoprecipitated AHF

FDA recall event 90353 · Class II · OneBlood, Inc.

Key facts

Event ID 90353
Recall numbers B-0436-2022
Recalling firm OneBlood, Inc.
Product type Biologics
Products Pooled Cryoprecipitated AHF
Classification Class II
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Misbranded Pooled Cryoprecipitated AHF was distributed.
Initiation date Apr 29, 2022
Report date Sep 28, 2022
Termination date Sep 21, 2022
City Orlando
State FL
Country United States
FEI number 1072425

At a glance

  • 1–9 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA drug and product recalls

FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.

Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

Browse all FDA drug and product recalls