Drug recall
Source Plasma
FDA recall event 42750 · Class II · Biomat USA, Inc.
Key facts
| Event ID | 42750 |
|---|---|
| Recall numbers | B-0324-13 |
| Recalling firm | Biomat USA, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected from a donor who received a piercing within one year of donation, was distributed. |
| Initiation date | Jun 19, 2006 |
| Report date | Nov 21, 2012 |
| Termination date | Nov 14, 2012 |
| City | Salt Lake City |
| State | UT |
| Country | United States |
| FEI number | 1773503 |
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: