Drug recall
Pooled Cryoprecipitated AHF
FDA recall event 78075 · Class III · OneBlood, Inc.
Key facts
| Event ID | 78075 |
|---|---|
| Recall numbers | B-0865-2017 |
| Recalling firm | OneBlood, Inc. |
| Product type | Biologics |
| Products | Pooled Cryoprecipitated AHF |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood components, not manufactured according to specifications, were distributed. |
| Initiation date | Aug 9, 2017 |
| Report date | Sep 20, 2017 |
| Termination date | Sep 12, 2017 |
| 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: