The Recall Desk
ModerateFDA (Devices)·Z-0244-2014·Announced 2013-11-20

Carestream Vue PACS Software Recall for Image Loading Issues

Carestream Health is recalling Vue PACS software because specific multi-slice images may fail to load in the viewer application.

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, which typically indicates a situation where use of the product may cause temporary or medically reversible health consequences. The specific hazard is a software defect preventing image loading, which is a functional failure rather than a direct physical injury risk.

Plain-English summary

Carestream Health, Inc. has issued a recall for the Carestream Vue PACS software. The recall involves specific client workstation versions, including 11.3.2.0, 11.3.2.4, and 11.4, with catalog number 8711459.

The recall is due to a software problem that may prevent some images from multi-slice studies, such as CT and MR, from loading into the viewer application under very specific conditions. This issue affects the system's ability to display certain medical images.

The affected products were distributed worldwide, including in the United States and internationally to Canada, Japan, and Kuwait. Users of the Carestream Vue PACS system should contact Carestream Health for further instructions on how to resolve the software issue.

The recalled product

Product
Carestream Vue PACS; UPG MX-O SVR 25K EX/YR UNLIMITED 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, retrieve

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 →