Hocoma AG: Medical Device Recall in 2020 - (Recall #: Z-2418-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: June 8, 2020

Date Posted: July 1, 2020

Recall Number: Z-2418-2020

Event ID: 85857

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.

Status: Ongoing

Product Quantity: 494

Code Information:

All units

Distribution Pattern:

Worldwide distribution - US Nationwide distribution including in the states of FL, GA, IL, MI, MN, MO, NE, NY, TX.

Voluntary or Mandated:

Voluntary: Firm initiated