Permobil Inc: M5 Corpus Power Wheelchair REF,120032
Read the official notice at FDA (device) →
The text below is copied from the official FDA (device) record. If anything differs, the official notice is correct.
- Company / brand
- Permobil Inc
- Product
- M5 Corpus Power Wheelchair REF,120032
- Reason / 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.
- Classification
- Class II
- Status
- Ongoing
- Distribution / 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.
- Recall initiated
- 2025-06-19
- Code info
- Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562
- Product quantity
- 715 wheelchairs
- Voluntary mandated
- Voluntary: Firm initiated
- City
- Lebanon
- State
- TN
- Country
- United States
- Event id
- 99267
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