Novarad Corporation: Medical Device Recall in 2016 - (Recall #: Z-2151-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

NovaPACS versions 7.4, 7.5, 7.6, and 8.0, Diagnostic Viewer. Distributed by Novarad Corporation. Picture archiving and communication system (PACS)

Product Classification:

Class II

Date Initiated: May 9, 2013

Date Posted: July 20, 2016

Recall Number: Z-2151-2016

Event ID: 74556

Reason for Recall:

Potential for images to be flipped while streaming, which could incorrectly display image orientation markers.

Status: Terminated

Product Quantity: 2695

Code Information:

All NovaPAC software versions 7.4, 7.5, 7.6, and 8.0

Distribution Pattern:

Worldwide distribution including US nationwide. No Canadian distribution.

Voluntary or Mandated:

Voluntary: Firm initiated