Drug recall
Source Plasma
FDA recall event 71781 · Class II · BPL Plasma, Inc. (Hot Springs)
Key facts
| Event ID | 71781 |
|---|---|
| Recall numbers | B-0895-15 |
| Recalling firm | BPL Plasma, Inc. (Hot Springs) |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, for which the donor was found not suitable for donation and product was not quarantined, was distributed. |
| Initiation date | Jun 23, 2015 |
| Report date | Sep 9, 2015 |
| Termination date | Aug 28, 2015 |
| City | Hot Springs |
| State | AR |
| Country | United States |
| FEI number | 1643463 |
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: