Reported Aug 5, 2026 · Ongoing · Updated Sep 16, 2026
M5 Corpus Power Wheelchair REF,120032
Permobil Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Permobil Inc · 300 Duke Dr · Lebanon, TN · 37090-8115
Is this the product you have?
M5 Corpus Power Wheelchair REF120032
- Lot codes and dates
- Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562
- Amount recalled
- 715 wheelchairs
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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