MAX MOBILITY, LLC
2 recall(s) on record — most severe on record: Class I.
Activity by year
- Recalls (2)
- Inspections (2)
Devices registered here (1)
- Wheelchair, PoweredProduct code ITI (opens in a new tab) · Class II · Physical Medicine · 21 CFR 890.3860
Recalls & enforcement
- Class IOngoing2025-08-12Due 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.
- Class IOngoing2024-12-20Due 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.
FDA inspections (2)
- NAI2023-12-07No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
- NAI2017-11-07No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “MAX MOBILITY, LLC (FEI 3008370857) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3008370857-max-mobility-llc/
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