Drug recall
Apheresis Platelets, Leukocytes Reduced, Irradiated
FDA recall event 74247 · Class II · American National Red Cross Southeastern Michigan Region
Key facts
| Event ID | 74247 |
|---|---|
| Recall numbers | B-0560-16 |
| Recalling firm | American National Red Cross Southeastern Michigan Region |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Apheresis product, for which the residual white blood cell count testing was not performed, was distributed. |
| Initiation date | Feb 11, 2016 |
| Report date | Jun 8, 2016 |
| Termination date | May 31, 2016 |
| City | Detroit |
| State | MI |
| Country | United States |
| FEI number | 1873044 |
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: