Official recall notice

FDA DeviceClass IINotable

FDA Recall: Vue Motion V12. Product Number: 1017979.

Recall date
2026-04-08
FDA class
Class II

Why it was recalled

Hazard

Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.

Recommended action

What to do

3,552 units

Product description

Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.

Verify with the official notice →
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