Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EPIQ 5 Ultrasound System with Pediatric Cardiology option Recalled by Philips Ultrasound, Inc. Due to When Epiq 5 Ultrasound System, WITH the Pediatric...
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 Ultrasound, Inc. directly.
Affected Products
EPIQ 5 Ultrasound System with Pediatric Cardiology option, Model: EPIQ 5G, EPIC 5C, EPIQ 5W. Catalog Number: 795204 / 795205. Part Number: 989605408541 With 453561736761 (1.1) 453561750041 (1.1.1) 453561753651 (1.1.2) 453561772231 (1.2) 453561772611 (1.2.1) 453561786571 (1.2.2) 453561785081 (1.3) 453561800581 (1.3.1) 453561805181 (1.3.2)
Quantity: 751 units total (246 units in the US and 505 units outside the US)
Why Was This Recalled?
When Epiq 5 Ultrasound System, WITH the Pediatric Cardiology option, is set up to Metric and weight and/or height is entered, a unit conversion error may result in the incorrect calculation of the patients Body Surface Area (BSA).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Ultrasound, Inc.
Philips Ultrasound, Inc. has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report