Permobil Inc recalls M5 Corpus Power Wheelchair REF
- Recalling company
- Permobil Inc
- Product
- M5 Corpus Power Wheelchair REF,120032
- Reason
- 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 – may cause temporary or medically reversible health consequences
- Recall date
- Jun 19, 2025
- Reported
- Aug 5, 2026
- 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.
- Status
- Ongoing
- Quantity
- 715 wheelchairs
- Lot / codes
- Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562
- Company location
- Lebanon, TN
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2805-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2805-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.