Z-2236-2023 Class II Ongoing
FDA device recall Z-2236-2023 was initiated by Trexo Robotics Holdings Inc. on May 31, 2023 and is designated Class II. 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. The recall status is ongoing. Affected quantity: 357 units.
Recall Details
- Product Type
- Devices
- Report Date
- August 2, 2023
- Initiation Date
- May 31, 2023
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 357 units
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.
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.
Code Information
All devices.