# FDA recall Z-1117-2025

> **Max Mobility LLC** · Class I · device recall initiated 2024-12-20.

## Product

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK  use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.

## Reason for recall

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.

## Distribution

US: AK	AL	AR	AZ	CA	CO	CT	DC	DE	FL	GA	HI	IA	ID	IL	IN	KS	KY	LA	MA	MD	ME	MI	MN	MO	MS	MT	NC	ND	NE	NH	NJ	NM	NV	NY	OH	OK	OR	PA	PR	RI	SC	SD	TN	TX	UT	VA	VT	WA	WI	WV	WY  OUS: Sweden, Canada, Australia, Japan, New Zealand, Colombia, Argentina, Hong Kong, Canada, Mexico, Bermuda, South Korea, Chile

## Key facts

- **Recall number:** Z-1117-2025
- **Recalling firm:** Max Mobility LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-12-20
- **Report date:** 2025-02-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lebanon, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1117-2025

## Citation

> AI Analytics. FDA recall Z-1117-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-1117-2025. Source: US FDA. Licensed CC0.

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