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FDA · Medical devicesClass I

Max Mobility LLC medical device recall: Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC…

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Medical devices
Classification
Class I
Status
Ongoing
Event ID
96086
Recall initiated
Dec 20, 2024
Classified by FDA
Feb 11, 2025
Posted in Enforcement Report
Feb 19, 2025
Recalling firm
Max Mobility LLC
Firm location
Lebanon, TN, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
E-Mail
Products in this event
2

What to do

Compare the product, lot or serial numbers below with what you have. If you use a prescription drug or medical device in this recall, talk to your pharmacist or health care provider before you stop using it, and follow the firm's instructions.

View the official FDA record ↗

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.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Dec 20, 2024. FDA classified it 53 days later, on Feb 11, 2025. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: 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 Max Mobility LLC has 2 recalls in our records.

Recalled products (2)

  • Z-1116-2025 Class I Ongoing

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

    Codes / lots: All serial numbers manufactured between August 17,2023 through November 21, 2024

    Quantity: unknown

  • Z-1117-2025 Class I Ongoing

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

    Codes / lots: All serial numbers manufactured between August 17,2023 through November 21, 2024

    Quantity: unknown

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA device enforcement dataset
Official notice
FDA Enforcement Report, event 96086
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.

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