Drug recall
Source Plasma
FDA recall event 82932 · Class III · Octapharma Plasma, Inc.
Key facts
| Event ID | 82932 |
|---|---|
| Recall numbers | B-0613-2019 |
| Recalling firm | Octapharma Plasma, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Source Plasma units, not meeting product specifications, were distributed. |
| Initiation date | May 13, 2019 |
| Report date | Jun 5, 2019 |
| Termination date | May 29, 2019 |
| City | Midfield |
| State | AL |
| Country | United States |
| FEI number | 3006718605 |
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: