medical MODERATE Updated 2026-08-05

Permobil Inc recalls M5 Corpus Power Wheelchair REF,120032

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Recalled Product

M5 Corpus Power Wheelchair REF,120032

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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