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Health product recall

IAMIN PRODUCTS (2015-04-30)

Starting date:
April 30, 2015
Posting date:
May 8, 2015
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-53289

Recalled Products

A. IAMIN PRODUCTS

Reason

The product for the IAMIN family of medical devices is not licenced in Canada. The associated products are the IAMIN moist dressing and the IAMIN hydrating gel.

Affected products

A. IAMIN PRODUCTS

Lot or serial number

More than 10 numbers, contact manufacturer.

Model or catalog number

GC044-1
M40329

Companies
Manufacturer
Photomedex Inc. also DBA Photo Therapeutics
147 Keystone Drive
Montgomeryville
18936
Pennsylvania
UNITED STATES