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IONTODERMA ID-1000 (2016-08-08)

Report a Concern
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