Drug recall
Apheresis Platelets, Platelet Additive Solution Added, Leukocytes Reduced
FDA recall event 82545 · Class II · The Blood Connection, Inc.
Key facts
| Event ID | 82545 |
|---|---|
| Recall numbers | B-0478-2019 |
| Recalling firm | The Blood Connection, Inc. |
| Product type | Biologics |
| Products | Apheresis Platelets, Platelet Additive Solution Added, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Apheresis product for which white blood cell count testing was not performed, was distributed. |
| Initiation date | Mar 2, 2019 |
| Report date | Apr 17, 2019 |
| Termination date | Apr 5, 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: