Z-2805-2026 Class II Ongoing
FDA device recall Z-2805-2026 was initiated by Permobil Inc on June 19, 2025 and is designated Class II. 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 uns… The recall status is ongoing. Affected quantity: 715 wheelchairs.
Recall Details
- Product Type
- Devices
- Report Date
- August 5, 2026
- Initiation Date
- June 19, 2025
- Termination Date
- N/A
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 715 wheelchairs
Product Description
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 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 CANADA.
Code Information
Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562