Drug recall
Source Plasma
FDA recall event 85727 · Class II · CSL PLASMA
Key facts
| Event ID | 85727 |
|---|---|
| Recall numbers | B-0513-2020 |
| Recalling firm | CSL PLASMA |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Source Plasma, collected in a manner that resulted in the test sample possibly being diluted with saline, was distributed. |
| Initiation date | Mar 16, 2020 |
| Report date | Jun 3, 2020 |
| Termination date | May 26, 2020 |
| City | Philadelphia |
| State | PA |
| Country | United States |
| FEI number | 3011813573 |
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: