M5 Corpus Power Wheelchair REF,120032

FDA device recall Z-2805-2026 · posted 2026-07-24 · Open, Classified

Recall details

Recalling firm

Permobil Inc

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.

Action taken

On June 10, 2025 Permobil issued a technical bulletin (recall notice) via Email to affected consignees. Permobil informed consignees of the following: 1. Cellular connection is required to receive and install the firmware update. 2. It is important to not use the wheelchair when the firmware update is in process (as indicated on the display of the input device). 3. Specific Remote Update Instructions are available if needed in addition to the on-screen information. 4. A confirmation of the completed update will be shown on the joystick display when the update successfully completes. 5. If you have any questions or concerns, please contact the Permobil Customer Experience team at (800) 736-0925. 1.

Root cause

Process design

Status

Open, Classified

Product code

ITI

Quantity affected

715 wheelchairs

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,

Date initiated

2025-06-19

Date posted

2026-07-24

Location

Lebanon, TN

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