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Medical Device

Vue Motion V12. Product Number: 1017979.

Recall date: 2026-04-08 · Source: FDA_DEVICE
Brand / Firm
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Product
Vue Motion V12. Product Number: 1017979.
Reason for recall
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
Units affected
3,552 units
Description
Vue Motion V12. Product Number: 1017979.
View official recall notice →