# FDA recall Z-2795-2026

> **Permobil Inc** · Class II · device recall initiated 2024-02-29.

## Product

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock  REF:120031, Model version 3

## Reason for recall

This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the wheelchair to tip over,

## 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 CAN.

## Key facts

- **Recall number:** Z-2795-2026
- **Recalling firm:** Permobil Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-02-29
- **Report date:** 2026-08-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Lebanon, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2795-2026

## Citation

> AI Analytics. FDA recall Z-2795-2026. Retrieved 2026-09-03 from https://api.ai-analytics.org/recall/Z-2795-2026. Source: US FDA. Licensed CC0.

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