Drug recall
Source Plasma
FDA recall event 53764 · Class II · Biomat USA, Inc
Key facts
| Event ID | 53764 |
|---|---|
| Recall numbers | B-0230-14 |
| Recalling firm | Biomat USA, Inc |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Donor Screening/Donor gave history which warranted deferral or follow up and was not deferred or follow up questions were not asked |
| Initiation date | Aug 1, 2009 |
| Report date | Jan 29, 2014 |
| Termination date | Jan 23, 2014 |
| City | Arlington |
| State | TX |
| Country | United States |
| FEI number | 3004036082 |
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 · Source date: