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FDAMarch 5, 2026device

Vue Motion V12. Product Number: 1017979.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

philips medical systems nederland b vphilipsphilips medical

UPCs

00884838100367008848381003430088483810033600884838100350

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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