FDAJuly 22, 2021device

EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Completed

Brands named

philips ultrasoundphilips

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi — Recall Details · AllClear