Drug recall
AllSet+" Gold HLA-A Low Res SSP, 54310D; UniTray¿ A Locus SSP, 7860010; UniTray¿ A Locus SSP w/ Taq, 7860110…
FDA recall event 67028 · Class II · Life Technologies Corporation
Key facts
| Event ID | 67028 |
|---|---|
| Recall numbers | B-0282-14 |
| Recalling firm | Life Technologies Corporation |
| Product type | Biologics |
| Products | AllSet+" Gold HLA-A Low Res SSP, 54310D; UniTray¿ A Locus SSP, 7860010; UniTray¿ A Locus SSP w/ Taq, 7860110; AllSet+" Gold HLA-ABC Low Res SSP, 54340D; UniTray¿ ABC SSP, 7800010; UniTray¿ ABC SSP w/… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | HLA typing assay, associated with false negative results, were distributed. |
| Initiation date | Sep 19, 2013 |
| Report date | Feb 19, 2014 |
| Termination date | Aug 5, 2014 |
| City | Brown Deer |
| State | WI |
| Country | United States |
| FEI number | 2244574 |
At a glance
- 1–9 Products in this recall
- 1–9 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 · Source date: