FDAClass IIAugust 5, 2026

Permobil M3 Corpus Power Wheelchair with Heavy Duty recall

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

Why was Permobil M3 Corpus Power Wheelchair with Heavy Duty 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,

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

All Units operating with firmware version 1.26.2/UDI:(01)17330818345674

Product
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Recalling firm
Permobil Inc
Quantity
140 units
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 CAN.
Recall date
August 5, 2026
Classification
Class II
Status
Ongoing
Agency
FDA (device)
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