FDAFDA recall Z-2805-2026 · Aug 5, 2026
Permobil Inc: M5 Corpus Power Wheelchair REF recall
Recall found
Product
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.
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
- Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562
- Quantity
- 715 wheelchairs
- 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.
- Recalling firm
- Permobil Inc, Lebanon, TN
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2025-06-19
Source: openFDA enforcement record Z-2805-2026 · search recall number Z-2805-2026 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.