# FDA recall Z-2805-2026

> **Permobil Inc** · Class II · device recall initiated 2025-06-19.

## 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

- **Recall number:** Z-2805-2026
- **Recalling firm:** Permobil Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-19
- **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-2805-2026

## Citation

> AI Analytics. FDA recall Z-2805-2026. Retrieved 2026-09-03 from https://api.ai-analytics.org/recall/Z-2805-2026. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*