The Recall Desk
ModerateFDA (Devices)·Z-0220-2014·Announced 2013-11-20

Carestream Vue PACS Software Recall for Image Loading Issues

Carestream Health is recalling Vue PACS software because a defect may prevent some CT and MR images from loading in the viewer.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: The recall is classified as FDA Class II, and the source text describes a software defect that may prevent image loading without reporting any injuries, illnesses, or deaths, fitting the criteria for a moderate severity voluntary precautionary recall.

Plain-English summary

Carestream Health, Inc. has issued a recall for the Carestream Vue PACS software, specifically the Virtual PWR Reading Basic SW StandAlone. The recall involves client versions 11.3.2.0, 11.3.2.4, and 11.4, with catalog number 8230633.

The recall was issued because a software problem may prevent some images from multi-slice studies, such as CT and MR, from loading into the viewer application under very specific conditions. The product is an image management system intended to archive, distribute, retrieve, and display images and data from hospital modalities.

The affected software was distributed worldwide, including in the United States and internationally to Canada, Japan, and Kuwait. Users of the affected software should contact Carestream Health for further instructions regarding the recall.

The recalled product

Product
Carestream Vue PACS; Virtual PWR Reading Basic SW StandAlone The CARESTREAM PACS is an image management system whose intended use is to provide completely scaleable local and wide area PACS solutions for hospital and related institutions/sites, which will archive, distribute, re

Distribution

Part of a larger recall action

This product is one of 50 recalled by Carestream Health Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 50 products in this recall →