Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced
FDA recall event 80493 · Class III · Blood Systems, Inc. DBA United Blood Services
Key facts
| Event ID | 80493 |
|---|---|
| Recall numbers | B-0755-2018 |
| Recalling firm | Blood Systems, Inc. DBA United Blood Services |
| Product type | Biologics |
| Products | Apheresis Red Blood Cells, Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which failed to meet product specifications, were distributed. |
| Initiation date | Jun 15, 2018 |
| Report date | Sep 5, 2018 |
| Termination date | Aug 24, 2018 |
| City | Lafayette |
| State | LA |
| Country | United States |
| FEI number | 2371456 |
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: