Drug recall
Source Plasma
FDA recall event 82232 · Class III · CSL Plasma, Inc
Key facts
| Event ID | 82232 |
|---|---|
| Recall numbers | B-0371-2019 |
| Recalling firm | CSL Plasma, Inc |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Source plasma products, for which donor eligibility screening was incorrectly performed, were distributed. |
| Initiation date | Dec 4, 2018 |
| Report date | Mar 20, 2019 |
| Termination date | Mar 13, 2019 |
| City | Gulfport |
| State | MS |
| Country | United States |
| FEI number | 3010978848 |
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: