Drug recall
Source Plasma
FDA recall event 49241 · Class III · ZLB Bioplasma, Inc.
Key facts
| Event ID | 49241 |
|---|---|
| Recall numbers | B-0345-13 |
| Recalling firm | ZLB Bioplasma, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which was collected from a donor in which donor suitability was not adequately determined, was distributed. |
| Initiation date | Jun 1, 2008 |
| Report date | Nov 21, 2012 |
| Termination date | Nov 14, 2012 |
| City | Tulsa |
| State | OK |
| Country | United States |
| FEI number | 1672443 |
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 · Source date: