Hocoma AG Industriestrasse 4 Volketswil Switzerland 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 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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
Brand
Hocoma AG Industriestrasse 4 Volketswil Switzerland
Lot Codes / Batch Numbers
All units
Products Sold
All units
Hocoma AG Industriestrasse 4 Volketswil Switzerland is recalling Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD ; 30004 LokomatPro L6.2 120V Kombi; 300 due to 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. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
The firm began notifying affected customers on June 8, 2020. Customers were informed that the motor-controller in their Lokomat may fail, potentially leading to an unintended error in functionality of the Body Weights Support Rope which means that the rope can go up or down in an uncontrolled way. To minimize a risk in relation to a potential failure of the motor-controller, the firm advises you to do the following: - As indicated in the Instruction for Use, permanently monitor patients, which perform a training with the Lokomat. The scenario is especially critical for pediatric patients. - In any case of unusual behavior of the Body Weight Support Rope (e.g. the rope goes up unintendedly) immediately press the Emergency button on the handrail or on the Tele Stop in order to stop the treadmill and the orthosis. Immediately afterwards switch off the power supply in order to stop the rope going up. Afterwards release the patient with the emergency release knob. See Details attached. - Make sure that all possible users of the Lokomat in your institution are informed of this temporary precautionary approach. The firm will continue to work on a technical solution to further minimize the risk of the potential motor control failure.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026