Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips EPIQ Diagnostic Ultrasound System Recalled by Philips Ultrasound Inc Due to Control panel arm assembly could have missing or...
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
Philips EPIQ Diagnostic Ultrasound System, Models EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx & EPIQ CVxi - Product Usage: the systems can assist the interventionist and surgeon with image guidance during treatment of cardiovascular disease in which the procedure uses both live X-ray and live Echo Guidance.
Quantity: 12,080 systems
Why Was This Recalled?
Control panel arm assembly could have missing or loose screws where undue force, pressure or weight is applied, the control panel mechanism can fail and break off.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Ultrasound Inc
Philips Ultrasound Inc has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report