FDAFDA recall Z-2795-2026 · Aug 5, 2026
Permobil Inc: Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031 recall
Recall found
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,
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your packaging. If this is a medicine or device you use, talk to your pharmacist or doctor before you stop or change anything, and contact the company or FDA for what to do with the product.
Recall details
- FDA classification
- Class II: use of or exposure to the product may cause temporary or medically reversible health problems, or the chance of serious problems is remote.
- Status
- Ongoing
- Codes, lots and dates
- All Units operating with firmware version 1.26.2/UDI:(01)17330818345674
- Quantity
- 140 units
- 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.
- Recalling firm
- Permobil Inc, Lebanon, TN
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2024-02-29
Source: openFDA enforcement record Z-2795-2026 · search recall number Z-2795-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 22, 2026, 4:56 AM EDT. The agency notice is the final word.