Official recall notice

FDA DeviceClass IINotable

FDA Recall: Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. In

Recall date
2026-08-19
FDA class
Class II

Why it was recalled

Hazard

Firmware issue potentially leading to loss of geometry movements.

Recommended action

What to do

4,252 units

Product description

Firmware issue potentially leading to loss of geometry movements.

Verify with the official notice →
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