Drug recall
Plasma Cryoprecipitated Reduced
FDA recall event 79777 · Class II · OneBlood, Inc.
Key facts
| Event ID | 79777 |
|---|---|
| Recall numbers | B-0510-2018 |
| Recalling firm | OneBlood, Inc. |
| Product type | Biologics |
| Products | Plasma Cryoprecipitated Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, for which the donor was incorrectly deleted from deferral list for vCJD travel history, was distributed. |
| Initiation date | Mar 13, 2018 |
| Report date | May 9, 2018 |
| Termination date | Apr 30, 2018 |
| City | St Petersburg |
| State | FL |
| Country | United States |
| FEI number | 1070196 |
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: