Drug recall
Apheresis Fresh Frozen Plasma
FDA recall event 75687 · Class II · BloodSource, Inc.
Key facts
| Event ID | 75687 |
|---|---|
| Recall numbers | B-0171-2017 |
| Recalling firm | BloodSource, Inc. |
| Product type | Biologics |
| Products | Apheresis Fresh Frozen Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Apheresis products, collected from a donor who was allowed to donate without a current physical, were distributed. |
| Initiation date | Oct 17, 2016 |
| Report date | Dec 7, 2016 |
| Termination date | Nov 28, 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: