RecallRadar

FDA Device recall Z-2267-2014

IntelePACS software versions 3-8-1 to 4-9-1, Product Usage: IntelePACS is a device that receives digital images and data from various sourc…

On 2014-08-27 the FDA classified a Class II recall of IntelePACS software versions 3-8-1 to 4-9-1, Product Usage: IntelePACS is a device that receives digital images and data from various sourc… by Intelerad Medical Systems, citing in specific situation a partially truncated file may be written to the IntelePACS server. This partially truncated file still can be viewed by InteleViewer and InteleViewer will r….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2267-2014
ClassificationClass II
Statusterminated
Initiated2014-07-03
Published2014-08-27
Last updated2026-09-13 11:53 UTC
CompanyIntelerad Medical Systems
DistributionUS

Product

IntelePACS software versions 3-8-1 to 4-9-1, Product Usage: IntelePACS is a device that receives digital images and data from various sources (such as, CT scanners, MRI scanners, ultrasound systems, R/F units, computer and direct radiographic devices, secondary capture devices, scanners, imaging gateways, or other imaging sources.

Reason

In specific situation a partially truncated file may be written to the IntelePACS server. This partially truncated file still can be viewed by InteleViewer and InteleViewer will report to the user that the file in question is complete. This situation only occurs if a file is partially truncated.

Identifiers

code_infosoftware versions 3-8-1 to 4-9-1

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2267-2014%22

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