Lasertubus Endotracheal Tube (2020-06-01)

Starting date:

June 1, 2020

Posting date:

June 16, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type I

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-73371

Last updated:
2020-10-16

• 
  Reason
• 
  Affected products

Affected Products

Lasertubus Endotracheal Tube

Reason

Recall related to complaints received regarding  the laser foil detaching from the tube.

Affected products