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FDA · Medical devices ·

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

Permobil Inc recalled Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3 on August 5, 2026 because of this recall has been reported retroactively. It was sold nationwide.

Why it was recalled

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,

What's recalled

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

Quantity: 140 units

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
Permobil Inc, Lebanon, TN
Date
Severity
Class II
the product could cause temporary or reversible health problems.
Where sold
Nationwide
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.
Status
Ongoing
Recall number
Z-2795-2026
Source
U.S. Food and Drug Administration

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