Drug recall
Platelets
FDA recall event 29515 · Class III · Gulf Coast Regional Blood Center
Key facts
| Event ID | 29515 |
|---|---|
| Recall numbers | B-1679-4 |
| Recalling firm | Gulf Coast Regional Blood Center |
| Product type | Biologics |
| Products | Platelets |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which was produced from a whole blood unit lacking phlebotomy documentation, was distributed. |
| Initiation date | Jul 1, 2003 |
| Termination date | Jul 28, 2004 |
| City | Houston |
| Country | United States |
| FEI number | 3002133806 |
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