Drug recall
BenchMark ULTRA and DISCOVERY ULTRA Instruments
FDA recall event 89727 · Class II · Ventana Medical Systems Inc
Key facts
| Event ID | 89727 |
|---|---|
| Recall numbers | Z-0894-2022 |
| Recalling firm | Ventana Medical Systems Inc |
| Product type | Devices |
| Products | BenchMark ULTRA and DISCOVERY ULTRA Instruments |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for Fluid Leak inside a staining system that could cause an electrical short circuit of the General Purpose Input/ Output Board's J1 Connector that could result in smoke and fire. |
| Initiation date | Jan 20, 2022 |
| Report date | Apr 13, 2022 |
| City | Oro Valley |
| State | AZ |
| Country | United States |
| FEI number | 1000125183 |
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 · Source date: