Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 75345 · Class II · American National Red Cross
Key facts
| Event ID | 75345 |
|---|---|
| Recall numbers | B-0056-2017, B-0057-2017 |
| Recalling firm | American National Red Cross |
| 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 did not meet the acceptable product specifications, were distributed. |
| Initiation date | Aug 7, 2016 |
| Report date | Oct 26, 2016 |
| Termination date | Oct 18, 2016 |
| City | Portland |
| State | OR |
| Country | United States |
| FEI number | 3072996 |
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: