FDA DeviceClass IINotable

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

Date: 2026-04-08
Brand: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Category: Medical Device
FDA Class: Class II

Description

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

Hazard

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

Remedy

3,552 units

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