IVES Disposable Conductive Plastic EEG Electrode CPE-23/D (2018-09-10)

Starting date:

September 10, 2018

Posting date:

September 28, 2018

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-67832

• 
  Reason
• 
  Affected products

Affected products

IVES Disposable Conductive Plastic EEG Electrode CPE-23/D

Reason

Product sold without a market authorization, a Medical Device Licence. Regulated party does not hold a Medical Device Licence for the sale of the product in Canada.

Affected products