Reported Jan 7, 2026 · Completed
Philips EPIQ Ultrasound Systems (various models) used in conjunction with the X5-1c transducer REF: , , 795200, 795201,…
Philips Ultrasound, LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.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 EPIQ Ultrasound Systems (various models) used in conjunction
- with the X5-1c transducer REF
795200795201795231795232795234
- REF
795117795122
- Lot codes and dates
- Software Version Numbers9.0, 9.01, 9.02 795234/UDI: (01)00884838107540 795232/UDI: (01)00884838107533 795231/
- UDI(01)00884838097933 795201/UDI: (01)00884838047693 795200/
- UDI(01)00884838107441 795122/
- UDI(01)00884838097933 795117/
- UDI(01)00884838047693
- Amount recalled
- 1,721 systems
Where it was sold
Why it was recalled
Retroactive: Ultrasound may experience an unexpected automatic reboot, resulting in damage to transducer.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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