FDA Device recall Z-2418-2020
Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD
- FDA Device
- Class II
- ongoing
- Published 2020-07-01
On 2020-07-01 the FDA classified a Class II recall of Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD by Hocoma Ag, citing 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 uncontro….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2418-2020 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2020-06-08 |
| Published | 2020-07-01 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Hocoma Ag |
| Distribution | US |
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
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.
Identifiers
| code_info | All units |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2418-2020%22
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