Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref:… — Class I medical device recall Z-2540-2025
Ongoing recall by Max Mobility LLC, reported 2025-09-24, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Due to a faulty electrical connection between the speed control Dial and the wheelchair motor, their is a pote
| Recall number | Z-2540-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Max Mobility LLC, Lebanon, TN, United States |
| Recall initiated | 2025-08-12 |
| Classified | 2025-09-12 |
| Reported by FDA | 2025-09-24 |
| Distributed | 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 |
| Quantity | 8,413 units |
| Model numbers | MX2-3DCMC |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2540-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.