The Recall Desk
ModerateFDA (Devices)·Z-0256-2014·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 temporary or medically reversible adverse health consequence. The specific hazard is a software defect preventing image loading, which is a functional failure rather than a direct physical injury or contamination risk.

Plain-English summary

Carestream Health, Inc. has issued a recall for the Carestream Vue PACS image management system. The recall involves specific client workstation software versions, including 11.3.2.0, 11.3.2.4, and 11.4, with catalog number 1738905.

The recall is due to a software problem where, under very specific conditions, some images from multi-slice studies such as CT and MR may not load into the viewer application. This issue affects the system's ability to display certain archived 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 resolving the software issue.

The recalled product

Product
Carestream Vue PACS; UPG MX-RAD SVR 7.5K 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, retrie

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 →