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Permobil Inc recalls M5 Corpus Power Wheelchair REF,120032
Recalled August 5, 2026 · FDA recall Z-2805-2026 · Permobil
Hazard
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. · FDA Class II
Units
715 wheelchairs
Sold at
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.
Description
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.
Product
M5 Corpus Power Wheelchair REF,120032
Manufacturer(s)
Permobil Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →