Drug recall
Source Plasma
FDA recall event 80823 · Class III · CSL Plasma Services, Inc.
Key facts
| Event ID | 80823 |
|---|---|
| Recall numbers | B-0785-2018 |
| Recalling firm | CSL Plasma Services, 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 screening was incorrectly performed, was distributed. |
| Initiation date | Mar 6, 2018 |
| Report date | Sep 19, 2018 |
| Termination date | Sep 7, 2018 |
| City | Melrose Park |
| State | IL |
| Country | United States |
| FEI number | 3005601555 |
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: