Drug recall
Apheresis Red Blood Cells, Leukocytes Reduced
FDA recall event 75748 · Class III · United Blood Services
Key facts
| Event ID | 75748 |
|---|---|
| Recall numbers | B-0219-2017 |
| Recalling firm | 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, in which quality control and distribution of products did not meet specifications, were distributed. |
| Initiation date | Oct 13, 2016 |
| Report date | Dec 28, 2016 |
| Termination date | Dec 21, 2016 |
| 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: