Drug recall
Gentueri Viral Transport Medium (VTM), Sterile, IVD
FDA recall event 89337 · Class II · Gentueri Inc
Key facts
| Event ID | 89337 |
|---|---|
| Recall numbers | Z-0504-2022 |
| Recalling firm | Gentueri Inc |
| Product type | Devices |
| Products | Gentueri Viral Transport Medium (VTM), Sterile, IVD |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Medium showed visual turbidity and discoloration, potentially contaminating samples transported for testing. |
| Initiation date | Mar 18, 2021 |
| Report date | Jan 26, 2022 |
| Termination date | Aug 28, 2023 |
| City | Verona |
| State | WI |
| Country | United States |
| FEI number | 3017528620 |
At a glance
- 1–9 Products in this recall
- None 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: