Drug recall
Source Plasma
FDA recall event 76833 · Class III · BPL Plasma, Inc
Key facts
| Event ID | 76833 |
|---|---|
| Recall numbers | B-0507-2017 |
| Recalling firm | BPL Plasma, Inc |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Plasma product, for which donor eligibility screening was incorrectly performed, was distributed. |
| Initiation date | Jan 18, 2017 |
| Report date | Apr 26, 2017 |
| Termination date | Apr 20, 2017 |
| City | Austin |
| State | TX |
| Country | United States |
| FEI number | 3006605566 |
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: