Health product recall

Portex Blue Line Ultra Tracheostomy Tube Inner Cannula (2019-02-10)

Starting date:
February 10, 2019
Posting date:
February 22, 2019
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-69118

Affected Products

Portex Blue Line Ultra Tracheostomy Tube Inner Cannula

Reason

8.00 mm ID part number 100/856/080, lot number 3578884, package incorrectly contained a 9.00 mm inner cannula.

Affected products

Portex Blue Line Ultra Tracheostomy Tube Inner Cannula

Lot or serial number
  • 3578884
Model or catalog number
  • 100/856/080
Companies
Manufacturer
Smiths Medical International Ltd.
Boundary Road
Hythe, Kent
CT21 6JL
UNITED KINGDOM