Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 76533 · Class II · American National Red Cross (the)
Key facts
| Event ID | 76533 |
|---|---|
| Recall numbers | B-0473-2017 |
| Recalling firm | American National Red Cross (the) |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, labeled as leukoreduced were not tested to verify the White Blood Cell count, were distributed. |
| Initiation date | Dec 12, 2016 |
| Report date | Apr 5, 2017 |
| Termination date | Mar 30, 2017 |
| City | West Henrietta |
| State | NY |
| Country | United States |
| FEI number | 3002957282 |
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: