Drug recall
Apheresis Fresh Frozen Plasma
FDA recall event 73111 · Class III · BloodSource, Inc.
Key facts
| Event ID | 73111 |
|---|---|
| Recall numbers | B-0291-16 |
| Recalling firm | BloodSource, Inc. |
| Product type | Biologics |
| Products | Apheresis Fresh Frozen Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Misbranded apheresis product was distributed. |
| Initiation date | Nov 25, 2015 |
| Report date | Feb 24, 2016 |
| Termination date | Feb 12, 2016 |
| City | Mather |
| State | CA |
| Country | United States |
| FEI number | 3007101464 |
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: