Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 73311 · Class II · American National Red Cross Great Lakes Region
Key facts
| Event ID | 73311 |
|---|---|
| Recall numbers | B-0356-16, B-0357-16 |
| Recalling firm | American National Red Cross Great Lakes Region |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, Apheresis Platelets, 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 the White Blood Cell count, were distributed. |
| Initiation date | Dec 29, 2015 |
| Report date | Mar 23, 2016 |
| Termination date | Mar 17, 2016 |
| City | Lansing |
| State | MI |
| Country | United States |
| FEI number | 1873033 |
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: