FDA recall, , Moderate risk
Philips Vue Motion V12
Vue Motion V12 may display image frames out of sequence during dynamic cine runs.
Summary by Recall Canary from the FDA notice
What happened
Philips Medical Systems Nederland B.V. of Best, Netherlands, began a recall of Vue Motion V12, Product Number 1017979, on March 5, 2026, because mis-ordered frames during dynamic cine runs may cause image frames to display out of sequence. The FDA added the recall to its Enforcement Report and classified it on March 27, 2026, and it was in the FDA's weekly enforcement report on April 8, 2026.
The recall affects 3,552 units distributed worldwide, including the US nationwide and many countries such as Algeria, Argentina, Australia, Canada, China, Germany, India, Japan, Mexico, and the United Kingdom.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the UDI-DI and product code listed under your product.
Incomplete list: 1,000 of 3,556 UDI-DIs shown.
A UDI-DI is the device identifier printed with the barcode on the device label.
Vue Motion V12.
- UDI-DI
- 00884838100367
- 00884838100343
- 00884838100336
- 00884838100350
- 20240923
- 86183662
- 118470289
- 115532146
- 115483951
- 117699552
- 86093591
- 98297412
- 86093647
- 86241626
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- 119288183
- 86241420
- 86326303
- 86325905
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- 108816071
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- Product code
- 1017979.
Recall details
- Company began the recall
- Sold in
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.
- Company
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Best, Netherlands
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98520
- Recall number
- Z-1692-2026
- Quantity recalled
- 3,552 units
All recalls from PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
