Reported Aug 5, 2026 · Ongoing

Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3

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?

  • Permobil M3 Corpus Power
  • Wheelchair with Heavy Duty Shock REF
    • 120031
    • Model version 3
Lot codes and dates
  • All Units operating with firmware version 1.26.2/UDI:(01)17330818345674
Amount recalled
140 units

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 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,

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Permobil Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 2:47 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.