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Open, Classified

All-round Joystick R-net Light. Electrical wheelchair component.

FDA Recall Z-2458-2025 · Posted 2025-09-02

Recalling Firmmo-Vis BVBA
Recall StatusOpen, Classified
Product CodeKNN
Date Initiated2025-07-10
Product Quantity3 units

Reason for Recall

Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.

Firm Action

An URGENT: MEDICAL DEVICE RECALL R-NET JOYSTICKS notification dated 07/10/2025 was sent to consignees instructing them to upgrade affected devices according to the provided Annex 2 or by emailing [email protected] to coordinate return. The software upgrade of affected devices should be conducted during the next scheduled annual maintenance of the joystick. These actions should be verified. Questions can be directed via email to [email protected] or by phone at +32 9 335 28 60.

Root Cause

Device Design

Distribution Pattern

US Nationwide distribution in the state of TX.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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