Z-2795-2026 Class II Ongoing
FDA device recall Z-2795-2026 was initiated by Permobil Inc on February 29, 2024 and is designated Class II. 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 w… The recall status is ongoing. Affected quantity: 140 units.
Recall Details
- Product Type
- Devices
- Report Date
- August 5, 2026
- Initiation Date
- February 29, 2024
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 140 units
Product Description
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 Pattern
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.
Code Information
All Units operating with firmware version 1.26.2/UDI:(01)17330818345674