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

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  Reason
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  Affected products

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