Permobil recalls M5 Corpus Power Wheelchair models with firmware 1.27-1.57 due to potential instability and unsafe driving conditions. Affected units may need firmware updates or repairs.
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.
Permobil is recalling M5 Corpus Power Wheelchairs with specific firmware versions because a missing safety feature could cause the chair to move unexpectedly under certain conditions. This poses a risk of instability and potential accidents if the wheelchair is used without proper safety measures.
The power platform firmware lacks specific drive inhibit logic, which can cause the wheelchair to move unexpectedly under restricted conditions. This may lead to unstable situations where the user could be at risk of injury if the wheelchair is not properly controlled.
Power wheelchair users who own the M5 Corpus model with firmware versions 1.27 through 1.57 are most at risk. This includes individuals who rely on this wheelchair for mobility.
Check if your M5 Corpus Power Wheelchair has firmware versions 1.27 through 1.57. The product is identified by the reference number REF,120032 and unique device identifier UDI-DI 17330818334562.
Identify your wheelchair's firmware version by checking the device settings or documentation.
Reach out to Permobil directly for firmware updates or repair options if your wheelchair is affected.
No, only those with firmware versions 1.27 through 1.57 and reference number REF,120032.
The official recall does not specify safe update procedures; contact Permobil directly for assistance.
Contact Permobil to arrange for a firmware update or repair, as the recall does not include a specific remedy.
We’ve drafted a message you can send Permobil to request your refund or repair — edit it as you like.
Subject: Recall Z-2805-2026 — Permobil Permobil Hello, I own a Permobil that is covered by recall Z-2805-2026 from Permobil. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
