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FDA · Medical devices ·

M5 Corpus Power Wheelchair REF,120032 recall

Permobil Inc recalled M5 Corpus Power Wheelchair REF,120032 on August 5, 2026 because of this recall is being reported retroactively. It was sold nationwide.

Why it was recalled

This recall is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, and may create an unstable condition in certain circumstances.

What's recalled

M5 Corpus Power Wheelchair REF,120032

Quantity: 715 wheelchairs

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 CANADA.
Status
Ongoing
Recall number
Z-2805-2026
Source
U.S. Food and Drug Administration

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