Hocoma Lokomat Pro Recalls: Uncontrolled Rope Movement Risk

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Recalling firmHocoma AGIndustriestrasse 4, N/A · Volketswil, N/A N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Hocoma is recalling specific models of Lokomat Pro devices because the motor controller might fail, causing the Body Weights Support Rope to move unpredictably. This poses a risk of injury during physical therapy sessions for patients with mobility issues.

Why it’s dangerous

The motor controller could malfunction, causing the Body Weights Support Rope to move up or down without control. This uncontrolled movement might lead to falls or injuries during physical therapy sessions for patients with mobility challenges.

Who’s affected

Patients using Lokomat Pro devices for therapy with walking disabilities are most at risk. The affected devices were sold to healthcare providers and therapists.

How to tell if you have this one

Check the catalog number on the device label. Affected models include 30003, 30004, 30005, 30683, 30684, and 32001.

Brand
Hocoma
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Device Label
Look for the catalog number on the device label to confirm if it is affected.

✎ GovInfoNow

Questions people ask

What models are recalled?

Lokomat Pro models with catalog numbers 30003, 30004, 30005, 30683, 30684, and 32001.

Why is this recall happening?

The motor controller may fail, causing the Body Weights Support Rope to move unpredictably, which could lead to injury during therapy sessions.

Is there a fix for this issue?

The recall record does not specify a remedy or fix.

Take action

Contact Hocoma

We’ve drafted a message you can send Hocoma to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-2418-2020 — Hocoma Hocoma

Hello,

I own a Hocoma that is covered by recall Z-2418-2020 from Hocoma.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-2418-2020 (June 8, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2418-2020 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Hocoma AG recalls Lokomat Pro, Catalog Numbers 30003 LokomatPro L6.2 120V AD ; 30004 LokomatPro L6.2 120V Kombi; 30005 LokomatPro L6.2

Use caution until it’s fixed