Ventana Medical Systems recalls

Recall found. Ventana Medical Systems is named in FDA Class II recall Z-2913-2026 covering navify Digital Pathology (on-prem) v2. Hazard: Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window Identifying details: navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material Number 09453733001 UDI-DI Code: 761333602095AQ Software version Numbers: 2.5.0, 2.5.0.1, 2.5.0.2, and 2.5.1. Status: Ongoing.

Models with recalls

navify Digital Pathology (on-prem) v2 (1)

All Ventana Medical Systems recalls

FDA Class II · Medical device · August 19, 2026

navify Digital Pathology (on-prem) v2 recall — Ventana Medical Systems, Inc.

Due to complaints received for the Image Management System regarding image/metadata discrepancy with the Viewer window

Official ID Z-2913-2026 · Official record ↗

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CPSC — consumer products ↗ (aggregated here)
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FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.