Drug recall
B17 SSP UniTray¿ Kit, REF 472303 and 472313; B Locus High Res SSP UniTray¿ Kit, REF 4730010 and 4730110…
FDA recall event 62468 · Class II · Life Technologies, Inc.
Key facts
| Event ID | 62468 |
|---|---|
| Recall numbers | B-2385-12 |
| Recalling firm | Life Technologies, Inc. |
| Product type | Biologics |
| Products | B17 SSP UniTray¿ Kit, REF 472303 and 472313; B Locus High Res SSP UniTray¿ Kit , REF 4730010 and 4730110; AllSet Gold SSP HLA-B17 High Res Kit, Prod.no. 541120D, AllSet Gold SSP HLA-B Locus High Res… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | HLA typing assay, associated with false negative results, was distributed. |
| Initiation date | May 18, 2012 |
| Report date | Aug 15, 2012 |
| Termination date | Nov 26, 2013 |
| 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: