Drug recall
Platelets
FDA recall event 30555 · Class II · LifeShare Inc
Key facts
| Event ID | 30555 |
|---|---|
| Recall numbers | B-0382-5 |
| Recalling firm | LifeShare Inc |
| Product type | Biologics |
| Products | Platelets |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which was manufactured from a whole blood unit in which the associated red blood cells was found to contain clots, was distributed. |
| Initiation date | Jun 23, 2004 |
| Termination date | Dec 22, 2004 |
| City | Elyria |
| Country | United States |
| FEI number | 1523639 |
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