Recall Z-2236-2023— Trexo Robotics Holdings Inc.

Name: FDA recall Z-2236-2023
Creator: U.S. Food and Drug Administration
Published: 2023-05-31

Class II · Ongoing

Class II FDA medical device recall by Trexo Robotics Holdings Inc., initiated 2023-05-31. FDA's recall record names no specific 510(k) clearance for this event. Product: Trexo Device. Reason: Electrical issues that could potentially render the device non-functional, give off electromagnetic influence to surrounding equipment, and risk of burns when in use..

Recalling firm: Trexo Robotics Holdings Inc.
Classification: Class II
Status: Ongoing
Initiated: 2023-05-31
Firm location: Mississauga, N/A, Canada

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.