Medical Device Recall: Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Permobil Inc · February 29, 2024
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.
States Affected
NATIONWIDE
Quantity Affected
140 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2795-2026
Status: ongoing
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