# FDA recall Z-2540-2025

> **Max Mobility LLC** · Class I · device recall initiated 2025-08-12.

## Product

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

## Reason for recall

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.

## 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: CAN, NZL, KOR, BMU, GBR, JPN, TWN, AUS, BRA, COL, MEX, ABW, SWE, CHL, ARG, HKG

## Key facts

- **Recall number:** Z-2540-2025
- **Recalling firm:** Max Mobility LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-12
- **Report date:** 2025-09-24

- **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-2540-2025

## Citation

> AI Analytics. FDA recall Z-2540-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2540-2025. Source: US FDA. Licensed CC0.

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