PlainRecalls
FDA Devices Moderate Class II Ongoing

Trexo Device

Reported: August 2, 2023 Initiated: May 31, 2023 #Z-2236-2023

Product Description

Trexo Device

Reason for Recall

Electrical issues that could potentially render the device non-functional, give off electromagnetic influence to surrounding equipment, and risk of burns when in use.

Details

Units Affected
357 units
Distribution
Worldwide distribution - US Nationwide and the countries of the Argentina, Australia, Brazil, Canada, China, Croatia, Czech Republic, England, Germany, India, Kuwait, Mexico, Poland, Qatar, Republic of Cyprus, Serbia, Singapore, Slovakia, Spain, United Arab Emirates, and Yemen.
Location
Mississauga, N/A

Frequently Asked Questions

What product was recalled?
Trexo Device. Recalled by Trexo Robotics Holdings Inc.. Units affected: 357 units.
Why was this product recalled?
Electrical issues that could potentially render the device non-functional, give off electromagnetic influence to surrounding equipment, and risk of burns when in use.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 2, 2023. Severity: Moderate. Recall number: Z-2236-2023.