FDA Medical devices recall ·
Vue Motion V12. Product Number: 1017979 recall
- Recall number
- Z-1692-2026
- Date
- (initiated March 5, 2026)
- Company / brand
- Philips Medical Systems Nederland B.V.
Veenpluis 4-6, Best, Netherlands - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 3,552 units
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
Vue Motion V12. Product Number: 1017979.
Why was it recalled?
Potential that mis-ordered frames in Vue Motion during dynamic cine runs may cause images frames to display out of sequence.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
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(
Distribution
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.
States: Puerto Rico
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-1692-2026. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.