Drug recall
Fresh Frozen Plasma
FDA recall event 32529 · Class II · American National Red Cross Indiana-Ohio Region
Key facts
| Event ID | 32529 |
|---|---|
| Recall numbers | B-2286-5, B-2287-5, B-2288-5, B-2289-5, B-2290-5, B-2291-5 |
| Recalling firm | American National Red Cross Indiana-Ohio Region |
| Product type | Biologics |
| Products | Fresh Frozen Plasma, Platelets, Red Blood Cells, Red Blood Cells (Apheresis) Leukocytes Reduced, Red Blood Cells Leukocytes Reduced and 1 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were untested for syphilis, were distributed. |
| Initiation date | May 4, 2005 |
| Termination date | Nov 1, 2005 |
| 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