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Munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application Smart Glasses Interface Wheelchair Head Control System

Official notice

12 Aug 2026

Last checked

22 Sept 2026

MediumFDA

An official FDA notice concerns Munevo. The notice reports a vehicle malfunction risk. Stop using the product and follow the official notice. Published 2026-08-12. Recall numbers: Z-2856-2026. Check the official notice for the complete list.

What to do now

Instructions for consumers are available in the official FDA notice.

Units affected

19

Recall number

Z-2856-2026

Official notice

2026-06-19

The hazard

Vehicle malfunction risk

How to check if you're affected

Compare the product name and identifiers below with the item you own. Follow the official notice if they match.

Other

UDI-DI 04260691380010

Event Ids

99328

Recall Numbers

Z-2856-2026

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Where it was sold

The source does not list specific retailers. See the official notice for where affected products were sold.

Location 1

US · United States

Affected area 1

US · United States

Affected area 2

CH · Switzerland

Affected area 3

DE · Germany

Affected area 4

ES · Spain

Affected area 5

GB · United Kingdom

Affected area 6

IT · Italy

Company & contacts

Brand

Manufacturer

Not provided

Phone

Not provided

Brand: Munevo. Contact: MUNEVO GMBH.

Source & status

Source

Tier

official

Category

ELECTRONICS

Classification

Class II

App estimate

medium

Recall details

Recall number

Z-2856-2026

Event id

99328

Units affected

19

Status

active

Classification

Class II

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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