Drug recall
PF24 Plasma
FDA recall event 82120 · Class II · Blood Systems, Inc.
Key facts
| Event ID | 82120 |
|---|---|
| Recall numbers | B-0317-2019 |
| Recalling firm | Blood Systems, Inc. |
| Product type | Biologics |
| Products | PF24 Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, for which donor eligibility screening was incorrectly performed, was distributed. |
| Initiation date | Nov 29, 2018 |
| Report date | Feb 27, 2019 |
| Termination date | Feb 20, 2019 |
| City | Scottsdale |
| State | AZ |
| Country | United States |
| FEI number | 2071464 |
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: