Health product recall

Dentronix Dry Heat Sterilizer (2019-11-07)

Starting date:
November 7, 2019
Posting date:
November 29, 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-71736

Last updated: 2019-12-02

Affected Products

Dentronix Dry Heat Sterilizer

Reason

A single Dentronix Dry Heat Sterilizer DDS7000 (p/n DDS7000115, serial number 190310642) was imported and sold into Canada without a valid medical device licence.

Affected products

Dentronix Dry Heat Sterilizer

Lot or serial number

190310642

Model or catalog number

DDS7000115

Companies
Manufacturer
Coltene/Whaledent, Inc.
235 Ascot Parkway
Cuyahoga Falls
44223
Ohio
UNITED STATES