Trexo Device — Class II medical device recall Z-2236-2023
Ongoing recall by Trexo Robotics Holdings Inc., reported 2023-08-02, distributed nationwide. Electrical issues that could potentially render the device non-functional, give off electromagnetic influence
| Recall number | Z-2236-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Trexo Robotics Holdings Inc., Mississauga, N/A, Canada |
| Recall initiated | 2023-05-31 |
| Classified | 2023-07-25 |
| Reported by FDA | 2023-08-02 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AU, BR, CA, CN, CY, CZ, DE, ES, GB, HR, IN, KW, MX, PL, QA, RS, SG, SK |
| Quantity | 357 units |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2236-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.