Drug recall
Source Plasma
FDA recall event 35600 · Class III · NABI
Key facts
| Event ID | 35600 |
|---|---|
| Recall numbers | B-1679-6 |
| Recalling firm | NABI |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor for whom post-donation information was received regarding a previous deferralfor unacceptable viral marker test results, were distributed. |
| Initiation date | Jan 20, 2005 |
| Termination date | Jul 7, 2012 |
| City | Gainesville |
| State | FL |
| Country | United States |
| FEI number | 1072432 |
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