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Max Mobility, LLC

Last updated September 17, 2026

Information

Device	Model / Reference	Registries	Class	Status
SmartDrive®	MX2+	FDA UDI	Class II	Active
SmartDrive®	MX2	FDA UDI	Class II	Active
Hiroller Elevating Wheelchair	K102837	FDA 510(k)	Class II	Active
Smartdrive Wheelchair Power-Assist	K113621	FDA 510(k)	Class II	Active
SmartDrive Wheelchair Power Assist	K151199	FDA 510(k)	Class II	Active

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Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Aug 12, 2025	Z-2538-2025	—	open, classified	Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
Aug 12, 2025	Z-2540-2025	—	open, classified	Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
Aug 12, 2025	Z-2539-2025	—	open, classified	Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a potential for lost of control of the device potentially resulting in minor or major injuries.
Dec 20, 2024	Z-1116-2025	—	open, classified	Due to faulty circuit board in speed control remote use in conjunction with a wheelchair power assist, their is a potential for lost of control of device potentially resulting in minor and major injuries.
Dec 20, 2024	Z-1117-2025	—	open, classified	Due to faulty circuit board in speed control remote use in conjunction with a wheelchair power assist, their is a potential for lost of control of device potentially resulting in minor and major injuries.