This page has been archived on the Web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

Intesys Clinical Suite (ICS) G2 Full/Smart Disclosure (2014-03-07)

Starting date:
March 7, 2014
Posting date:
April 4, 2014
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-38677

Recalled Products

  1. Intesys Clinical Suite (ICS) G2 Full/Smart Disclosure

Reason

Inform about defect in the ICS G2 Clinical Access software CD. The programs installed on the clinical access CD are incorrect and will prevent from installing clinical access. No one has been injured as a result of this issue and no data on the database is at risk.

Affected products

A. Base de données cliniques Intesys Clinical Suite (ICS) G2 – Full/Smart Disclosure

Lot or serial number
  • 063-1829-11
Model or catalog number
  • 92810
Companies
Manufacturer

Spacelabs Healthcare Inc.

35301 SE Center Street

Snoqualmie

98065

Washington

UNITED STATES