This page has been archived on the Web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.
GlideScope Titanium LoPro and MAC Single use (2016-01-04)
- Starting date:
- January 4, 2016
- Posting date:
- January 22, 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-56768
Affected Products
- GlideScope Titanium LoPro Single Use
- GlideScope Titanium MAC Single Use
Reason
Potential for flickering (intermittent break-up of the on-screen video image) in the video laryngoscopy image when GlideScope Titanium SU laryngoscope blades are in use.
Affected products
A. GlideScope Titanium LoPro Single Use
Lot or serial number
lots 081114 to 090315; lots 081814 to 103015
Model or catalog number
- 0574-0130
- 0574-0131
Companies
- Manufacturer
-
Verathon Medical (Canada) ULC
2227 Douglas Road
Burnaby
V5C 5A9
British Columbia
CANADA
B. GlideScope Titanium MAC Single Use
Lot or serial number
lots 022514 to 101915; lots 072314 to 101515
Model or catalog number
- 0574-0132
- 0574-0133
Companies
- Manufacturer
-
Verathon Medical (Canada) ULC
2227 Douglas Road
Burnaby
V5C 5A9
British Columbia
CANADA