Health product recall

AngeLite System - Main Unit (2019-10-31)

Starting date:
October 31, 2019
Posting date:
November 15, 2019
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-71613

Last updated: 2019-11-15

Affected Products

AngeLite System - Main Unit

Reason

New revised copies of this Manual would be sent to all customers / users that are using the Angelite System in Canada.

Affected products

AngeLite System - Main Unit

Lot or serial number

All codes.

Model or catalog number

ANGELITE SDC/DDC

Companies
Manufacturer

ADVANCED TECHNOLOGY LASER CO., LTD

920 JIANCHUAN ROAD

A2-5F, SHANGHAI, SHANGHAI

200240

CHINA