Trexo Home and Trexo Plus
Brand(s)
Last updated
Summary
Product
Trexo Home and Trexo Plus
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Affected products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| Trexo Home | More than 10 numbers, contact manufacturer. | A0001 |
| Trexo Plus | More than 10 numbers, contact manufacturer. | A0001 |
Issue
The following malfunctions and nonconformances were observed during Trexo lab-testing and Trexo design reviews of the device, Resulting in this voluntary device recall and proposed field correction. Electromagnetic (EM) radiation levels above threshold (Ref: IEC 60601-1-11), as observed during lab-testing contracted by Trexo. Water ingress was observed within electronics enclosures after IP22 testing, as observed during lab-testing contracted by Trexo.
Recall start date: July 31, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Physical medicine
Companies
Trexo Robotics Inc.
6705 Milcreek Drive, Mississauga, Ontario, Canada, L5N 5M4
Published by
Health Canada
Audience
General public
Recall class
Type II
Identification number
RA-74192
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