FDA recall record

Omnyx Digital Pathology System (DPS) Software version 1.1 The Omnyx" Integrated Digital recall — FDA Z-0469-2014

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…

Class IIclassification
Z-0469-2014official record ID
Dec 18, 2013report date

Recall record at a glance

Official recordZ-0469-2014
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmOmnyx LLC
Report dateDec 18, 2013
Recall initiation dateOct 1, 2013
Quantity2
LocationPittsburgh, PA, United States

Official product description

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.

Why the product was recalled

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.

Distribution information

International Distribution to Canada and Switzerland only.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

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