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Health product recall

Dermalight 80 Psoracomb (2013-04-08)

Starting date:
April 8, 2013
Posting date:
March 20, 2014
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-38445

Recalled Products

Dermalight 80 Psoracomb

Reason

Wrong user manual sent with device.

Affected products

Dermalight 80 Psoracomb

Lot or serial number

UVB-080

Model or catalog number

7839

Companies
Manufacturer
National Biological Corporation
23700 Mercantile Road
Beachwood
44122
Ohio
UNITED STATES