Drug recall
Source Plasma
FDA recall event 48953 · Class III · Biomat USA, Inc.
Key facts
| Event ID | 48953 |
|---|---|
| Recall numbers | B-0220-13 |
| Recalling firm | Biomat USA, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor who was previously deferred, were distributed. |
| Initiation date | Mar 17, 2008 |
| Report date | Dec 5, 2012 |
| Termination date | Nov 26, 2012 |
| City | Portland |
| State | OR |
| Country | United States |
| FEI number | 3005600120 |
At a glance
- 1–9 Products in this recall
- 1–9 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 · Source date: