- Recalling firm
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Reason for recall
- Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
- Affected products (lot / model / serial)
- Product Number: 1017979, Software Version: v12.2.0 - 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: 86183662, 118470289, 115532146, 115483951, 117699552, 86093591, 98297412, 86093647, 86241626, 86093616, 119288183, 86241420, 86326303, 86325905, 86325795, 86325794, 86325747, 86325221, 86093571, 108816071, 86093582, 86093358, 86093539, 86241707, 86241692, 86093595, 86241861, 86241751, 86241678, 86324616, 116468394, 106682968, 86241742, 87750382, 108664430, 118757545, 87751135, 87750882, 86325445, 86241699, 86241684, 86241669, 86241750, 86093376, 89412152, 86093502, 86369383, 86093605, 120505331, 86093623, 86093339, 86093663, 86093678, 86367969, 104418433, 86325612, 86093588, 86093356, 86324563, 86093674, 86093646, 86093566, 86093685, 86093659, 118007768, 107808460, 119061786, 86093547, 88168079, 86326302, 86325187, 86325123, 86093545, 86093435, 86093427, 95752135, 94477265, 92029774, 92029787, 87771660, 117645555, 117645550, 86241704, 86241689, 86241674, 107639091, 112190786, 112190691, 86093283, 106771488, 110432369, 110432367, 106771482, 119091432, 119091431, 118487430, 118487429, 97582725, 97582724, 97582723, 97582653, 97582719, 97582717, 97582716, 87940696, 107632484, 116468405, 106410735, 117979657, 86241787, 86241771, 107327494, 107327505, 118832692, 99601715, 99601713, 94677044, 92107086, 118239830, 117908479, 97223395, 96789905, 116645253, 116645227, 99601477, 99601462, 101939624, 101939623, 108423189, 108423187, 112368329, 94774385, 118905692, 115619712, 108420051, 86097812, 117795737, 95364241, 86097897, 119690483, 119690374, 119690229, 119690557, 108374575, 86097930, 86097807, 86367896, 94645462, 94645430, 94645536, 94644301, 94644110, 95364465, 86097900, 86097899, 86097870, 86097869, 86097867, 86097866, 86097865, 86097864, 86097872, 86097797, 93942911, 86097968, 95864471, 95863241, 95862554, 95861090, 95857876, 95857299, 95857238, 95856111, 116036959, 108387852, 108387818, 108387787, 108385798, 108385775, 108385742, 86097888, 92994681, 92994630, 92994624, 92994574, 92994546, 92994507, 92994368, 92993154, 92993151, 92993146, 92992839, 92992837, 92994642, 92993515, 86097956, 86097802, 86097795, 86097958, 86097957, 86097885, 86097884, 86097912, 86097911, 86097910, 86097874, 99156870, 86242184, 95635728,
- Units affected
- 3,552 units
- Distribution pattern
- Worldwide distribution - US Nationwide and the countries of Algeria, Andorra, Angola, Argentina, Australia, Austria, Belgium, Bolivia, Brazil, Cambodia, Canada, Chile, China, Colombia, Costa Rica, Cyprus, Czech Republic, Denmark, Dominican Republic, Ecuador, Egypt, Estonia, Finland, France, Germany, Gibraltar, Greece, Guernsey, Holy See (Vatican City State), Honduras, Hungary, Iceland, India, Indonesia, Ireland, Israel, Italy, Japan, Jersey, Jordan, Kuwait, Lebanon, Malaysia, Mexico, Morocco, Netherlands, New Zealand, Norway, Oman, Palestine, State of, Panama, Papua New Guinea, Peru, Philippines, Poland, Portugal, Puerto Rico, Qatar, Romania, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Thailand, United Arab Emirates, United Kingdom, Uruguay, Viet Nam, Zambia.
- Firm location
- Best, Netherlands
- Recall type
- Voluntary: Firm initiated
- How the firm notified customers
- Letter
- Product type
- Devices
- Status
- Ongoing
- Recall number
- Z-1692-2026
- Recall initiated
- March 5, 2026
- FDA classification date
- March 27, 2026
- FDA report date
- April 8, 2026
- FDA event ID
- 98520
- Last updated on HTM Vibe
- July 24, 2026