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Health product recall

Waterlase Express All-Tissue Laser System

Starting date:
June 5, 2017
Posting date:
June 21, 2017
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-63694

Reason

Incorrect footswitch pairing instructions were provided with Waterlase Express All-Tissue Laser System.

Affected products

Waterlase Express All-Tissue Laser System

Lot or serial number

71701034
71701036
71703018
72161286

Model or catalog number

7210001

Companies

Manufacturer
Biolase, Inc.
4 Cromwell
Irvine
92618
California
UNITED STATES