# FDA recall Z-2236-2023

> **Trexo Robotics Holdings Inc.** · Class II · device recall initiated 2023-05-31.

## Product

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

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.

## Key facts

- **Recall number:** Z-2236-2023
- **Recalling firm:** Trexo Robotics Holdings Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-31
- **Report date:** 2023-08-02

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mississauga, N/A, Canada

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2236-2023

## Citation

> AI Analytics. FDA recall Z-2236-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2236-2023. Source: US FDA. Licensed CC0.

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