Drug recall
Cryoprecipitated AHF
FDA recall event 91477 · Class II · Oklahoma Blood Institute
Key facts
| Event ID | 91477 |
|---|---|
| Recall numbers | B-0136-2023 |
| Recalling firm | Oklahoma Blood Institute |
| Product type | Biologics |
| Products | Cryoprecipitated AHF |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood product, for which donor eligibility was incomplete, was distributed. |
| Initiation date | Nov 23, 2022 |
| Report date | Jan 18, 2023 |
| Termination date | Jan 12, 2023 |
| City | Oklahoma City |
| State | OK |
| Country | United States |
| FEI number | 1626009 |
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: