Drug recall
Platelets, Pathogen Reduced
FDA recall event 75721 · Class II · ARUP Laboratories, Inc.
Key facts
| Event ID | 75721 |
|---|---|
| Recall numbers | B-0204-2017 |
| Recalling firm | ARUP Laboratories, Inc. |
| Product type | Biologics |
| Products | Platelets, Pathogen Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, in which component preparation was not prepared in accordance with specifications, was distributed. |
| Initiation date | Oct 3, 2016 |
| Report date | Dec 21, 2016 |
| Termination date | Dec 9, 2016 |
| City | Sandy |
| State | UT |
| Country | United States |
| FEI number | 1720911 |
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: