Rusch Greenlite (2020-01-15)

Starting date:

January 15, 2020

Posting date:

January 31, 2020

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-72227

Last updated: 2020-07-10

• Reason
• Affected products

Affected Products

Rusch Greenlite

Reason

Teleflex has received complaints that the lights guide of the Rusch Greenlite Mac Laryngoscope broke at the point of a welded joint either prior to use during setup or during use inside the patients mouth.

Affected products