Greenlight Laser Fibers (2020-03-30)

Starting date:

March 30, 2020

Posting date:

April 17, 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-72829

Last updated: 2020-04-17

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  Reason
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  Affected products

Affected Products

Greenlight Laser Fibers

Reason

Internal bench testing has determined that an increased irrigation flow may increase the liquid cooling effect and may reduce temperature related complaints

Affected products