Recall Z-1692-2026— PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Name: FDA recall Z-1692-2026
Creator: U.S. Food and Drug Administration
Published: 2026-03-05

Class II · Ongoing

Class II FDA medical device recall by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V., initiated 2026-03-05. It names one FDA 510(k) clearance: K151774. Product: Vue Motion V12. Product Number: 1017979.. Reason: Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence..

Recalling firm: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Classification: Class II
Status: Ongoing
Initiated: 2026-03-05
Firm location: Best, Netherlands

510(k) clearances named in this recall

1 on FDA's record

K151774 — CARESTREAM Vue MotionCarestream Health, Inc.·cleared 2015-09-21

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.