Vue Motion V12 Imaging System
Philips Vue Motion V12 (1017979) may display image frames out of sequence during dynamic imaging runs.
Contact Philips Medical Systems for guidance on frame-ordering verification and potential software updates or service checks for your Vue Motion V12 system.
Recall at a glance
- Quantity recalled
- 3,552 units
Why it was recalled
Philips Vue Motion V12 (Product Number 1017979) may display image frames out of sequence during dynamic cine runs due to potential frame mis-ordering. This could result in clinicians viewing cardiac or other dynamic imaging data in incorrect temporal order, affecting diagnostic accuracy. Affected units have worldwide distribution.
Is mine affected?
Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.
Vue Motion V12. Product Number: 1017979.
- UDI-DI
- 00884838100367, 00884838100367, 00884838100343, 00884838100367, 00884838100367, 00884838100367, 00884838100343, 00884838100367, 00884838100343, 00884838100336, 00884838100367, 00884838100350, 00884838100367, 00884838100350, 00884838100343, 00884838100350, 00884838100367, 00884838100336, 00884838100336, 00884838100336
Where it was sold
Distributed nationwide.
Timeline
- Firm initiated recall
- Publicly announced
- Listed on Recall Canary
- Summary updated
Official source
Other recent recalls from PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Editorial summary by Recall Canary · summary updated 2026-04-27 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification