Drug recall
Whole Blood for Manufacture of Non-Injectables
FDA recall event 31415 · Class II · Interstate Blood Bank Inc dba Knoxville Plasma Center
Key facts
| Event ID | 31415 |
|---|---|
| Recall numbers | B-1063-5 |
| Recalling firm | Interstate Blood Bank Inc dba Knoxville Plasma Center |
| Product type | Biologics |
| Products | Whole Blood for Manufacture of Non-Injectables |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which tested repeatedly reactive for the antibody to hepatitis C virus (anti-HCV), was distributed. |
| Initiation date | Mar 11, 2004 |
| City | Knoxville |
| Country | United States |
| FEI number | 1045035 |
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