This page has been archived on the Web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.
INTELEPACS (2017-11-30)
- Starting date:
- November 30, 2017
- Posting date:
- December 14, 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, Hospitals, General Public
- Identification number:
- RA-65418
Affected products
INTELEPACS
Reason
Following a complaint from a client, Intelerad is taking a pro-active field action to prevent occurrence of a possible patient safety problem at client sites. The issue is triggered by the presence of the "less than" character (
Affected products
INTELEPACS
Lot or serial number
Version 4-1-1 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
)>