Drug recall
Source Plasma
FDA recall event 72064 · Class III · BPL Plasma, Inc.
Key facts
| Event ID | 72064 |
|---|---|
| Recall numbers | B-0039-16 |
| Recalling firm | BPL Plasma, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor for whom there was no documentation of checking the arm, mouth, or general appearance on the day of donation, were distributed. |
| Initiation date | Jul 22, 2015 |
| Report date | Oct 14, 2015 |
| Termination date | Oct 5, 2015 |
| City | Clearwater |
| State | FL |
| Country | United States |
| FEI number | 3000215056 |
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: