Drug recall
Recovered Plasma
FDA recall event 31896 · Class II · Blood Bank of Alaska, Inc.
Key facts
| Event ID | 31896 |
|---|---|
| Recall numbers | B-1329-5, B-1330-5 |
| Recalling firm | Blood Bank of Alaska, Inc. |
| Product type | Biologics |
| Products | Recovered Plasma, Red Blood Cells, Leukocytes Removed, Irradiated, Washed |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, that tested negative for hepatitis, but were collected from an ineligible donor due to a history of jaundice, were distributed., Bood products, that tested negative for hepatitis, but were collected from an ineligible donor due to a history of jaundice, were distributed. |
| Initiation date | Oct 27, 2003 |
| Termination date | Jun 24, 2005 |
| City | Anchorage |
| Country | United States |
| FEI number | 3071403 |
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