Official recall notice

FDA DeviceClass IINotable

FDA Recall: M5 Corpus Power Wheelchair REF,120032

Recall date
2026-08-05
FDA class
Class II

Why it was recalled

Hazard

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.

Product description

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.

Affected products

Power Platform firmware versions 1.27 through 1.57 UDI-DI 17330818334562

Verify with the official notice →
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