Drug recall
Source Plasma
FDA recall event 83446 · Class II · CSL Plasma, Inc.
Key facts
| Event ID | 83446 |
|---|---|
| Recall numbers | B-0848-2019 |
| Recalling firm | CSL Plasma, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood product, prepared without the appropriate amount of additive solution, was distributed. |
| Initiation date | Jun 6, 2019 |
| Report date | Sep 11, 2019 |
| Termination date | Aug 30, 2019 |
| City | Las Vegas |
| State | NV |
| Country | United States |
| FEI number | 3014378670 |
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: