FDA Device Intelligence
HomeDevice types › KNN

Components, Wheelchair

FDA product code KNN · Class 1 · Physical Medicine

1,217
Registered devices
291
Adverse events
11
Recalls
64
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2026-06-19MUNEVO GMBHA software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected steering drift
2025-07-10mo-Vis BVBADevices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check
2025-07-10mo-Vis BVBADevices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check
2025-07-10mo-Vis BVBADevices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check
2025-07-10mo-Vis BVBADevices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check
2025-07-10mo-Vis BVBADevices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check
2025-07-10mo-Vis BVBADevices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check
2023-11-28mo-Vis BVBAIn rare cases, the lever of the throttle can get temporarily stuck during the movement and does not come back to its neutral point by itself. If this happens du
2023-07-06Aquila CorporationDefective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.
2023-07-06Aquila CorporationDefective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.