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Terminated

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.

FDA Recall Z-0469-2014 · Posted 2013-12-09

Recalling FirmOmnyx Llc
Recall StatusTerminated
Product CodeOTU
Date Initiated2013-10-01
Date Terminated2014-04-16
Product Quantity2

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.

Firm Action

Omnyx sent a Urgent Field Safety Notice letter dated October 1, 2013, to all affected customers. The letter identified the product the problem and the action needed to be taken by the customers. Please discontinue use of the measurement and area calculation features of the annotation tools (line, rectangle/square, ellipse/circle, and freeform) in the DPS Image Viewer at this time. If any of these tools have been used for measurements or area calculations on clinical cases, verify measurements and calculations on glass slides. Please confirm receipt of these instructions by completing the attached form and scanning/emailing it to FieldAction@ omnyx.com or faxing it to 001-412-894-2137 Product Correction: An updated version of the DPS SW will be released and installed on your system as soon as it becomes available. Please note that the appropriate regulatory authorities have been informed of this field action. We apologize for any inconvenience that this may have caused you and are working diligently to address this issue. If you have any additional questions or concerns, please contact you GE Healthcare account representative. Further questions please call (412) 891-2100.

Root Cause

Software design

Distribution Pattern

International Distribution to Canada and Switzerland only.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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