This page has been archived on the Web

Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.

Health product recall

INTELEPACS (2017-09-25)

Starting date:
September 25, 2017
Posting date:
November 22, 2017
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type II
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
Healthcare Professionals, General Public, Hospitals
Identification number:
RA-65184

Affected products

INTELEPACS

Reason

Intelerad has identified a software problem with the magnification glass tool which, in some instances, displays a different image than the one currently being shown in the selected viewport.

Affected products

INTELEPACS

Lot or serial number

Version 3-5-1 and up.

Model or catalog number

INTELEPACS

Companies
Manufacturer
Intelerad Medical Systems Incorporated
895 De La Gauchetiere Street West, 4th floor
Montreal
H3B 4G1
Quebec
CANADA