Wet-Field Coagulator (2018-02-09)

Starting date:

February 9, 2018

Posting date:

February 22, 2018

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-66040

• Reason
• Affected products

Affected products

Wet-Field Coagulator

Reason

The correct device was sold, labelled with the wrong information regarding the gage size.

Affected products