Z-0469-2014 Class II Terminated
FDA device recall Z-0469-2014 was initiated by Omnyx Llc on October 1, 2013 and is designated Class II. 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 calculatio… The recall status is terminated (terminated April 16, 2014). Affected quantity: 2.
Recall Details
- Product Type
- Devices
- Report Date
- December 18, 2013
- Initiation Date
- October 1, 2013
- Termination Date
- April 16, 2014
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 2
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.
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.
Distribution Pattern
International Distribution to Canada and Switzerland only.
Code Information
catalog # OMN-1005056-1, K1600LH, DPS 1.1