Drug recall
Recovered Plasma
FDA recall event 28133 · Class III · Heartland Blood Centers
Key facts
| Event ID | 28133 |
|---|---|
| Recall numbers | B-0691-4 |
| Recalling firm | Heartland Blood Centers |
| Product type | Biologics |
| Products | Recovered Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, that was not properly quarantined after the donor reported a post donation illness, was distributed. |
| Initiation date | Oct 23, 2003 |
| Termination date | Feb 18, 2004 |
| City | Aurora |
| Country | United States |
| FEI number | 1470274 |
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