Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 82560 · Class II · The Blood Connection, Inc.
Key facts
| Event ID | 82560 |
|---|---|
| Recall numbers | B-0489-2019, B-0490-2019 |
| Recalling firm | The Blood Connection, Inc. |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, Apheresis Red Blood Cells, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were labeled as leukoreduced but were not tested to verify white blood cell count, were distributed. |
| Initiation date | Feb 20, 2019 |
| Report date | Apr 24, 2019 |
| Termination date | Apr 12, 2019 |
| City | Piedmont |
| State | SC |
| Country | United States |
| FEI number | 1048067 |
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: