Drug recall
Source PlasmaSource Plasma
FDA recall event 32520 · Class II · Milwaukee Blood Plasma,Inc
Key facts
| Event ID | 32520 |
|---|---|
| Recall numbers | B-0240-6 |
| Recalling firm | Milwaukee Blood Plasma,Inc |
| Product type | Biologics |
| Products | Source PlasmaSource Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Source Plasma, which tested positive for human immunodeficiency virus (HIV- 1/2), was distributed. |
| Initiation date | Mar 27, 2002 |
| Termination date | Dec 2, 2005 |
| City | Milwaukee |
| Country | United States |
| FEI number | 2176255 |
At a glance
- 1–9 Products in this recall
- 10–99 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