Drug recall
Platelets
FDA recall event 31766 · Class III · Oklahoma Blood Institute - Sylvan N Goldman Center
Key facts
| Event ID | 31766 |
|---|---|
| Recall numbers | B-1266-5 |
| Recalling firm | Oklahoma Blood Institute - Sylvan N Goldman Center |
| Product type | Biologics |
| Products | Platelets |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which may have been prepared from a Whole Blood unit with an extended collection time, was distributed. |
| Initiation date | Dec 19, 2003 |
| Termination date | Jun 7, 2005 |
| City | Oklahoma City |
| Country | United States |
| FEI number | 1626009 |
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