Drug recall
Source Plasma
FDA recall event 75624 · Class II · BPL Plasma, Inc.
Key facts
| Event ID | 75624 |
|---|---|
| Recall numbers | B-0169-2017 |
| Recalling firm | BPL Plasma, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed. |
| Initiation date | Jul 29, 2016 |
| Report date | Dec 7, 2016 |
| Termination date | Nov 28, 2016 |
| City | Beaumont |
| State | TX |
| Country | United States |
| FEI number | 3003190471 |
At a glance
- 1–9 Products in this recall
- 1–9 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: