Recalls and alerts more than 4 years old are automatically archived. While this information can still be accessed in the database, it has not been altered or updated since it was archived. Web pages that are archived on the Web are not subject to the Government of Canada Web Standards. As per the Communications Policy of the Government of Canada, you can request alternate formats by contacting us.

IONTODERMA ID-1000 (2016-08-08)

Starting date:
August 8, 2016
Posting date:
August 10, 2016
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-59758

Affected products

A. IONTODERMA ID-1000

Reason

Failed to comply to the section 26 of the medical devices regulations by selling medical devices without proper licenses.

Affected products

A. IONTODERMA ID-1000

Lot or serial number

All lots

Model or catalog number

N/A

Companies
Manufacturer
IONTODERMA
2305 RUE GUENETTE
MONTREAL
H4R 2E9
Quebec
CANADA