Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EPIQ Ultrasound Systems Recalled by Philips Ultrasound Inc Due to Ultrasound system control panel arm swivel lock could...
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 Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi
Quantity: 8935
Why Was This Recalled?
Ultrasound system control panel arm swivel lock could fail, which could cause the control panel and monitor to swivel freely while a user is positioning the monitor, or transporting/moving the system, which could lead to patient or user musculoskeletal injury.
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