This page has been archived on the Web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.
Intellispace ECG (2014-08-06)
- Starting date:
- August 6, 2014
- Posting date:
- August 22, 2014
- 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-41125
Recalled Products
Intellispace ECG
Reason
Philips has become aware that if multiple Quinton stress ECG records are being processed during IECG import at the same time, it is possible that the XML patient ID from one patient can be incorrectly linked to a report from a second patient that is in the processing queue.
Affected products
Intellispace ECG
Lot or serial number
- US31400041
- US31400046
- USN1300020
Model or catalog number
860426
Companies
- Manufacturer
-
Philips Medical Systems
3000 Minuteman Road
Andover
01810
Massachusetts
UNITED STATES