Intelerad Medical Systems: Medical Device Recall in 2014 - (Recall #: Z-2267-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: July 3, 2014

Date Posted: August 27, 2014

Recall Number: Z-2267-2014

Event ID: 68719

Reason for Recall:

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.

Status: Terminated

Product Quantity: 230

Code Information:

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

Distribution Pattern:

Worldwide Distribution - USA Nationwide and the countries of Scotland, Ireland, United Kingdom, Canada, Australia, and New Zealand.

Voluntary or Mandated:

Voluntary: Firm initiated