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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66596

1 recalled-product record grouped only because every row carries this exact official event ID.

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Event summary

Timeline bucket
October 01, 2013
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Omnyx Llc

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 1

Digital Pathology System (DPS) Software version 1.1 The Omnyx" Integrated Digital Pathology system, which consists of a whole slide scanner and associated software applications, is a scanning, receiving, storing, managing, annotating and computer monitor viewing system for digital whole slide images. Omnyx" products are for in vitro diagnostic use for specific clinical applications, and are intended for research use only on other applications. Specific clinical use applications are indicated in separate clinical specific user guides supplied by Omnyx.

Z-0469-2014
Recall number
Z-0469-2014
Initiated
October 01, 2013
Classification
Class II
Status
Terminated
Recalling firm
Omnyx Llc
Quantity
2

App-derived interpretation

Device software or design reason.device_software_design · v1.0.0
issue associated with Digital Pathology System (DPS) Software

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

There is an issue associated with Digital Pathology System (DPS) Software, in which the annotation tools within the DPS version 1.1 Image Viewer will display incorrect measurements and area calculations for a region of interest on a scanned slide, under certain conditions.

Code information

catalog # OMN-1005056-1, K1600LH, DPS 1.1

Distribution pattern

International Distribution to Canada and Switzerland only.

Field note

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