This page has been archived on the Web

Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.

Health product recall

Myobrace and MRC Trainers (2014-12-12)

Starting date:
December 12, 2014
Posting date:
March 27, 2015
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-52683

Recalled Products

A. Myobrace

B. MRC Trainers

Reason

Devices were misclassified as Class I but are Class II. Devices were incorrectly sold into canada without an appropriate device licence issued by Health Canada.

Affected products

A. Myobrace

Lot or serial number

Not applicable

Model or catalog number

MYOBRACE

Companies
Manufacturer

MYOFUNCTIONAL RESEARCH CO.

PO BOX 7699, GOLD COAST MAIL CENTER

BUNDA

9999

AUSTRALIA



B. MRC Trainers

Lot or serial number

Not applicable

Model or catalog number

MRC TRAINERS

Companies
Manufacturer

MYOFUNCTIONAL RESEARCH CO.

PO BOX 7699, GOLD COAST MAIL CENTER

BUNDA

9999

AUSTRALIA