Drug recall
Panoscreen I, II, III
FDA recall event 31484 · Class III · Immucor Inc
Key facts
| Event ID | 31484 |
|---|---|
| Recall numbers | B-0123-6 |
| Recalling firm | Immucor Inc |
| Product type | Biologics |
| Products | Panoscreen I, II, III |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Panoscreens, packaged with the incorrect Master List, were distributed. |
| Initiation date | Sep 19, 2003 |
| Termination date | Nov 30, 2005 |
| City | Norcross |
| Country | United States |
| FEI number | 1034569 |
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