Drug recall
Fresh frozen plasma.
FDA recall event 29401 · Class II · American National Red Cross Indiana-Ohio Region
Key facts
| Event ID | 29401 |
|---|---|
| Recall numbers | B-1811-4, B-1812-4, B-1813-4, B-1814-4, B-1815-4 |
| Recalling firm | American National Red Cross Indiana-Ohio Region |
| Product type | Biologics |
| Products | Fresh frozen plasma., Platelets, Leukocytes Reduced, Recovered plasma., Red Blood Cells, Leukocytes Reduced, Red blood cells, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected in a manner were the sterility of the products may have been compromised, were distributed. |
| Initiation date | Dec 9, 2003 |
| City | Fort Wayne |
| Country | United States |
| FEI number | 1873031 |
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