Drug recall
navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5…
FDA recall event 98998 · Class II · Ventana Medical Systems, Inc.
Key facts
| Event ID | 98998 |
|---|---|
| Recall numbers | Z-2913-2026 |
| Recalling firm | Ventana Medical Systems, Inc. |
| Product type | Devices |
| Products | navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material Number 09453733001 UDI-DI Code: 761333602095AQ In the United States, navify Digital… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window |
| Initiation date | Apr 20, 2026 |
| Report date | Aug 19, 2026 |
| City | Tucson |
| 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: