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Health product recall

Theradome LH80 Pro Laser Helmet (2014-10-05)

Starting date:
October 5, 2014
Posting date:
January 22, 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-56752

Affected Products

Theradome LH80 Pro Laser Helmet

Reason

The Theradome LH80 PRO Laser Helmet, a medical device, is not licenced by Health Canada.

Affected products

Theradome LH80 Pro Laser Helmet

Lot or serial number

More than 10 numbers, contact manufacturer

Model or catalog number

LH80 PRO

Companies
Manufacturer

Theradome, Inc.

4900 HOPYARD ROAD, SUITE 100

Pleasanton

94588

California

UNITED STATES