Trexo Robotics Holdings Inc.: Medical Device Recall in 2023 - (Recall #: Z-2236-2023)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Trexo Device

Product Classification:

Class II

Date Initiated: May 31, 2023

Date Posted: August 2, 2023

Recall Number: Z-2236-2023

Event ID: 92563

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.

Status: Ongoing

Product Quantity: 357 units

Code Information:

All devices.

Distribution Pattern:

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.

Voluntary or Mandated:

Voluntary: Firm initiated