Drug recall
Apheresis Platelets, Leukocytes Reduced, Irradiated
FDA recall event 76316 · Class II · American National Red Cross (the)
Key facts
| Event ID | 76316 |
|---|---|
| Recall numbers | B-0324-2017 |
| Recalling firm | American National Red Cross (the) |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced, Irradiated |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Platelet products, for which WBC quality control testing was not performed, were distributed. |
| Initiation date | Dec 19, 2016 |
| Report date | Feb 15, 2017 |
| Termination date | Feb 3, 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: