Merge PACS

Starting date:

August 26, 2016

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-60232

• Reason
• Affected products

Affected Products

Merge PACS

Reason

This recall has been initiated because the cross reference lines a.k.a cut lines or localizer lines may not display properly. This is due to math error when calculating the cut line position for studies with extremely high precision in The Dicom Tag Image Orientation Patient (0020, 0037) containing values of greater than 15 significant digits. When the problem is encountered the cross reference lines will move erratically as the user stack scrolls through the study.

Affected products