Drug recall
Platelets Pheresis
FDA recall event 31221 · Class II · West Tennessee Regional Blood Center Inc
Key facts
| Event ID | 31221 |
|---|---|
| Recall numbers | B-0817-5 |
| Recalling firm | West Tennessee Regional Blood Center Inc |
| Product type | Biologics |
| Products | Platelets Pheresis |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected from a donor whose arm scrub was incorrectly performed, was distributed. |
| Initiation date | Dec 27, 2003 |
| Termination date | Mar 29, 2005 |
| City | Jackson |
| Country | United States |
| FEI number | 1071200 |
At a glance
- 1–9 Products in this recall
- None 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