HIGHFDA DEVICE

Max Mobility/Permobil Recalls 25,389 MX2+ SpeedControl Dial Units (2025)

Max Mobility LLC and Permobil recalled 25,389 MX2-3DC SpeedControl Dial units used with the SmartDrive MX2+ wheelchair power assist. A faulty electrical connection between the speed control dial and the wheelchair motor can cause loss of control. Users should stop using the device immediately and follow the manufacturer’s recall instructions for next steps.

Official notice

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
August 12, 2025
Status
ACTIVE
Severity
8/10

Quick Facts at a Glance

Recall Date
August 12, 2025
Hazard Level
HIGH
Brands
Max Mobility, Permobil
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
Nationwide (50 states)
At-Risk Groups
GENERAL, ELDERLY, PREGNANT

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Max Mobility, Permobil
Product type
Power wheelchair speed control dial
Model numbers
MX2-3DC, MX2+ SmartDrive
Sold at
Multiple Retailers
Where affected
Nationwide

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    August 12, 2025

  2. Reported by FDA DEVICE

    September 24, 2025

  3. RecallRadar source check

    April 18, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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.

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Max Mobility LLC or your healthcare provider for instructions. Notification method: Letter

About This Product

The SmartDrive MX2+ is a wheelchair power assist system designed to help users propel heavy chairs with motorized assistance. The SpeedControl Dial MX2-3DC adjusts or governs speed settings for the device.

Why This Is Dangerous

A faulty electrical connection can cause intermittent or complete loss of control of the wheelchair during operation, increasing the risk of injury to the user.

Industry Context

This recall is not described as part of a broader industry pattern in the provided materials.

Real-World Impact

Users may experience unexpected chair movement or an inability to stop, potentially resulting in injuries. The recall affects many units across multiple countries, signaling a cross-border safety concern.

Practical Guidance

How to identify if yours is affected

  1. Identify your MX2-3DC SpeedControl Dial on the SmartDrive MX2+ system.
  2. Confirm the model is MX2-3DC used with SmartDrive MX2+.
  3. Review the serial numbers for units distributed between April 25, 2022 and July 8, 2025.
  4. If affected, stop using the device immediately.

Where to find product info

Recall details are published on the FDA enforcement page linked in the notice. The recall number is Z-2538-2025.

What timeline to expect

Manufacturers typically complete refunds or replacements within 4-8 weeks after the recall notice is issued and validated.

If the manufacturer is unresponsive

  • Document all communications
  • Escalate to consumer protection agencies if the maker does not respond within a reasonable time frame
  • Consider contacting a healthcare provider or supplier for interim guidance

How to prevent similar issues

  • Check for recall notices before purchasing wheelchair accessories.
  • Ask providers for recall history of any mobility aids.
  • Maintain updated contact with manufacturers for recall notifications.

Documentation advice

Retain the recall letter, invoices, model numbers, serial numbers, and all correspondence with the manufacturer for records.

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

Product Details

Model numbers/serials: MX2-3DC SpeedControl Dial in conjunction with SmartDrive MX2+ Wheelchair Power Assist. All serial numbers distributed between April 25, 2022 and July 8, 2025. Distribution: United States across multiple states and U.S. territories listed; international distribution includes CAN, NZL, KOR, BMU, GBR, JPN, TWN, AUS, BRA, COL, MEX, ABW, SWE, CHL, ARG, HKG.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • MX2-3DC SpeedControl Dial
  • Distributed April 25, 2022 to July 8, 2025
  • US and international distribution
  • Class I recall
  • High hazard level

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALELDERLYPREGNANT
Injury Types
ELECTRICALFALLCRUSHING

Product Details

Model Numbers
MX2-3DC
MX2+ SmartDrive
Affected States
Nationwide
Report Date
September 24, 2025
Recall Status
ACTIVE

Related Recalls

Health & Personal Care
MEDIUM

AvKARE Recalls Rosuvastatin Tablets Due to Dissolution Issues

AvKARE recalled 7,991 cartons of Rosuvastatin Tablets on December 31, 2025. The recall stems from the product being out of specification for dissolution. Consumers should stop using the medication immediately and consult healthcare providers for guidance.

SUN PHARMACEUTICAL INDUSTRIES
Labeling: Not
Read more