Reported Oct 28, 2026 · Ongoing · Updated Nov 2, 2026
Philips Lumify Diagnostic Ultrasound System
Philips Ultrasound, LLC
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips Ultrasound, LLC · 22100 Bothell Everett Hwy · Bothell, WA · 98021-8431
Is this the product you have?
- Philips Lumify Diagnostic Ultrasound System
- Lot codes and dates
- UDI-DI/Software Version
Android: 00884838122116/1.X3.X4.X5.X
- iOS00884838124141/2.X and 5.X
- UDI-DI/Software Version
- Amount recalled
- 13,206
Where it was sold
Why it was recalled
Stop using this product now
Ultrasound system may: 1) Not recognize previous transducer registration, prevent scanning, require re-registration with Wi-Fi/cellular access, which may be unavailable outside of the hospital (ambulances/aircraft/field); 2) At connection between transducer USB cable to tablet/phone, there may be an unstable connection/may disconnect disrupting function. May cause diagnosis/treatment delay.
Using this product could cause serious injury, illness or death — stop using it now.
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