Drug recall
Platelets.
FDA recall event 48046 · Class III · Michigan Community Blood Center
Key facts
| Event ID | 48046 |
|---|---|
| Recall numbers | B-1633-08 |
| Recalling firm | Michigan Community Blood Center |
| Product type | Biologics |
| Products | Platelets. |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, for which the quality control testing was incomplete, were distributed. |
| Initiation date | Feb 25, 2008 |
| Termination date | Jul 17, 2008 |
| City | Traverse City |
| State | MI |
| Country | United States |
| FEI number | 1000517886 |
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