Recall
FDAHealthJune 19, 2025

Permobil Inc — M5 Corpus Power Wheelchair REF,120032

⚠️ 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.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
June 19, 2025

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.

What's affected?

Product
M5 Corpus Power Wheelchair REF,120032
Lot code
Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562

Additional details

Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 715 wheelchairs.

View original FDA notice →

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