Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EPIQ 7 Ultrasound System 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
EPIQ 7 Ultrasound System, Model 795200, 795201, 795202. Intended for diagnostic ultrasound imaging and fluid flow analysis.
Quantity: 306 units total (206 international; 100 in the US).
Why Was This Recalled?
A problem has been detected with Philips Model EPIQ 7 Ultrasound System, software version 1.0 and 1.0.1. Using the International System Date Format may result in calculation errors in Gestational Age Gestational Age (GA) and Established Due Date (EDD).
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