Drug recall
Source Plasma
FDA recall event 79929 · Class II · Octapharma Plasma, Inc.
Key facts
| Event ID | 79929 |
|---|---|
| Recall numbers | B-0518-2018 |
| Recalling firm | Octapharma Plasma, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Source Plasma unit, not meeting product specifications, was distributed. |
| Initiation date | Feb 14, 2018 |
| Report date | May 2, 2018 |
| Termination date | Apr 26, 2018 |
| City | North Little Rock |
| State | AR |
| Country | United States |
| FEI number | 3007960042 |
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: