Health product recall

Mercury (Long pulsed Nd:YAG laser) (2019-05-12)

Starting date:
May 12, 2019
Posting date:
May 24, 2019
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-70029



Last updated: 2019-05-24

Affected Products

Mercury (Long pulsed Nd:YAG laser)

Reason

The device is unlicensed in Canada.

Affected products

Mercury (Long pulsed Nd:YAG laser)

Lot or serial number

All lots.

Model or catalog number

MERCURY

Companies
Manufacturer

WON TECH CO., LTD

64 TECHNO 8-RO, YUSEONG-GU

DAEJEON

SOUTH KOREA