Data Foundry

Medical device recalls 2025

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref:… — Class I medical device recall Z-1117-2025

Ongoing recall by Max Mobility LLC, reported 2025-02-19, distributed in AK, AL, AR, AZ, CA, CO, CT, DC…. Due to faulty circuit board in speed control remote use in conjunction with a wheelchair power assist, their i

Recall numberZ-1117-2025
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmMax Mobility LLC, Lebanon, TN, United States
Recall initiated2024-12-20
Classified2025-02-11
Reported by FDA2025-02-19
DistributedAK, 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
Countries outside the USAR, AU, BM, CA, CL, CO, HK, JP, KR, MX, NZ, SE
Model numbersMX2-3DCK

Product

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

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.

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-1117-2025. 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.