Drug recall
Source Plasma
FDA recall event 28771 · Class II · BioLife Plasma Services LP
Key facts
| Event ID | 28771 |
|---|---|
| Recall numbers | B-1217-4 |
| Recalling firm | BioLife Plasma Services LP |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Source Plasma, which tested negative for the hepatitis B surfact antigen (HBsAg), but was collected from a donor who subsequently tested repeatedly reactive for HBsAg, was distributed. |
| Initiation date | Jan 31, 2001 |
| Termination date | May 28, 2004 |
| City | Fayetteville |
| Country | United States |
| FEI number | 3000204650 |
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