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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