HIGHFDA DEVICE

M5 Corpus Power Wheelchair REF,120032

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.

PermobilHealth & Personal CareMedical DevicesPower Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DEVICE
Recall date
June 19, 2025
Status
ACTIVE

Quick Facts at a Glance

Recall Date
June 19, 2025
Hazard Level
HIGH
Brand
Permobil
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Permobil
Model numbers
Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    June 19, 2025

  2. Reported by FDA DEVICE

    August 5, 2026

  3. RecallRadar source check

    August 12, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

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 You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Permobil Inc or your healthcare provider for instructions. Notification method: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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Full Description

M5 Corpus Power Wheelchair REF,120032. Reason: 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.. Classification: Class II. 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.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562
Affected States
ALL
Report Date
August 5, 2026
Recall Status
ACTIVE