Lokomat Pro — Class II medical device recall Z-2418-2020
Ongoing recall by Hocoma AG, reported 2020-07-01, distributed nationwide. The motor controller may fail, which can potentially lead to an error in functionality of the Body Weights Sup
| Recall number | Z-2418-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Hocoma AG, Volketswil, N/A, Switzerland |
| Recall initiated | 2020-06-08 |
| Classified | 2020-06-23 |
| Reported by FDA | 2020-07-01 |
| Distributed | Nationwide (US) |
| Quantity | 494 |
| Reason classes | device malfunction |
| Model numbers | 30003 |
Product
Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD ; 30004 LokomatPro L6.2 120V Kombi; 30005 LokomatPro L6.2 120V PE; 30683 LokomatPro L6.2 110V FD PE; 30684 LokomatPro L6.2 110V FD Kombi; 32001 LokomatPro L6.2 110V FD AD Product Usage: The intended use of the Lokomat is to support treadmill training to treat patients with walking disabilities caused by neurological, muscular or bone-related disorders. isokinetic testing and evaluation system
Reason for recall
The motor controller may fail, which can potentially lead to an error in functionality of the Body Weights Support Rope, which means that the rope can go up or down in an uncontrolled way.
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-2418-2020. 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.