FDA recall Z-2805-2026

Permobil Inc · Class II · device

Product

M5 Corpus Power Wheelchair REF,120032

Reason for recall

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.

Distribution

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.

Key facts

Status
Ongoing
Initiation date
2025-06-19
Report date
2026-08-05
Voluntary/Mandated
Voluntary: Firm initiated
Location
Lebanon, TN, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2805-2026