Reported Apr 8, 2026 · Ongoing
Vue Motion V12. Product Number: 1017979.
Philips Medical Systems Nederland B.v.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 4-6 · Best · N/A
Is this the product you have?
- Vue Motion V12
- Product Number1017979
- Lot codes and dates
- Product Number1017979
- Software Versionv12.2.0 - v12.2.8.500
- UDI Numbers
(01)00884838100367(11)200221(10)12.2.5(01)00884838100367(11)230223(10)12.2.8.300(01)00884838100343(11)200423(10)12.2.5.0(01)00884838100367(11)230615(10)12.2.8.310(01)00884838100367(11)200903(10)12.2.5.1(01)00884838100367(11)230720(10)12.2.8.400(01)00884838100343(11)201125(10)12.2.5.100(01)00884838100367(11)230921(10)12.2.8.410(01)00884838100343(11)210217(10)12.2.5.200(01)00884838100336(11)231221(10)12.2.8.420(01)00884838100367(11)210628(10)12.2.5.300(01)00884838100350(11)240116(10)12.2.8.421(01)00884838100367(11)210628(10)12.2.5.300(01)00884838100350(11)240204(10)12.2.8.422(01)00884838100343(11)220525(10)12.2.5.400(01)00884838100350(11)240226(10)12.2.8.424(01)00884838100367(11)230223(10)12.2.5.405(01)00884838100336(11)231221(10)12.2.8.420(01)00884838100336(11)230301(10)12.2.5.406(01)00884838100336(11)231221(10)12.2.8.420(01)00884838100367(11)230320(10)12.2.5.407(01)00884838100336(11)231221(10)12.2.8.420(01)00884838100367(11)230403(10)12.2.5.408(01)00884838100367#(11)231223(10)12.2.8.435(01)00884838100343(11)240211(10)12.2.5.413(01)00884838100367#(11)231228(10)12.2.8.435A(01)00884838100343(11)20240923(10)12.2.5.414(01)00884838100343(11)240917(10)12.2.8.436(01)00884838100343(11)250728(10)12.2.5.416(01)00884838100367(11)241014(10)12.2.8.437(01)00884838100367(11)210308(10)12.2.8.0(01)00884838100343(11)241128(10)12.2.8.438(01)00884838100367(11)220127(10)12.2.8.100(01)00884838100367(11)250122(10)12.2.8.439(01)00884838100343(11)220417(10)12.2.8.130(01)00884838100350(11)240407(10)12.2.8.440(01)00884838100350(11)221213(10)12.2.8.200(01)00884838100367(11)210308(10)12.2.8.0(01)00884838100350(11)230301(10)12.2.8.210(01)00884838100367(11)240616(10)12.2.8.500
- Equipment Number
2,932 of 2,932 codes
861836621184702891155321461154839511176995528609359198297412860936478624162686093616119288183862414208632630386325905863257958632579486325747863252218609357110881607186093582860933588609353986241707862416928609359586241861862417518624167886324616116468394106682968862417428775038210866443011875754587751135877508828632544586241699862416848624166986241750860933768941215286093502863693838609360512050533186093623860933398609366386093678863679691044184338632561286093588860933568632456386093674
- Amount recalled
- 3,552 units
This recall covers 23 products
The agency filed one notice per product. You are reading one of them; the other 22 are below.
10 more are in the archive.
Where it was sold
- Nationwide
- PR
Why it was recalled
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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