Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound Recalled by Philips Medical Systems North America Inc. Due to A problem has been detected with Philips Model...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips Medical Systems North America Inc. directly.
Affected Products
Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound imaging and fluid flow analysis. Catalogue numbers 795200 / 795201 / 795202 / 795204 / 795205 / 795206 EPIQ is intended for diagnostic ultrasound imaging and fluid flow analysis. The collection of Doppler velocity results values are used to assist in diagnosing the existence, location and severity of cardiac or vasculare stenosis.
Quantity: 489 total =227 units in US and 262 units Internationally (no Canadian consignees)
Why Was This Recalled?
A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound System. The system will report incorrect Doppler velocities if you use High Pulse Repetition Frequency (HPRF) with multiple sample volume gates. While in High Pulse Repetition Frequency (HPRF) in Display Zoom Velocity Scale using manual spectral Doppler trace, the velocities in the velocity results table may be overstated by
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Medical Systems North America Inc.
Philips Medical Systems North America Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report