Drug recall
Plasma
FDA recall event 35444 · Class II · Amer. National Red Cross-Greater Chesapeake & Potomac Reg.
Key facts
| Event ID | 35444 |
|---|---|
| Recall numbers | B-0219-7, B-0220-7 |
| Recalling firm | Amer. National Red Cross-Greater Chesapeake & Potomac Reg. |
| Product type | Biologics |
| Products | Plasma, Red Blood Cells |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which tested negative for the antibody to the human immunodeficiency virus (anti-HIV- 1/2), but were collected from a donor who provided post donation information regarding having a… |
| Initiation date | Feb 9, 2006 |
| Termination date | Dec 6, 2006 |
| City | Baltimore |
| Country | United States |
| FEI number | 1173011 |
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