FDA recall Z-2795-2026

Permobil Inc · Class II · device

Product

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

Reason for recall

This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the wheelchair to tip over,

Distribution

Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, WV, WY and the country of CAN.

Key facts

Status
Ongoing
Initiation date
2024-02-29
Report date
2026-08-05
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lebanon, TN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2795-2026