Permobil Inc recalls Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031
- Recalling company
- Permobil Inc
- Product
- Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
- Reason
- 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,
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Feb 29, 2024
- 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 CAN.
- Status
- Ongoing
- Quantity
- 140 units
- Lot / codes
- All Units operating with firmware version 1.26.2/UDI:(01)17330818345674
- Company location
- Lebanon, TN
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-2795-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-2795-2026 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.