FDAMarch 28, 2016device

EPIQ DIAGNOSTIC ULTRASOUND SYSTEM, Model EPIQ 5C, EPIC 5G, EPIQ 5W, EPIQ 7C, EPIC 7GC, and EPIQ 7W. Diagnostic Ultrasound System for ultrasound imaging in abdominal, cardiac adult, cardiac other (fetal), cardiac pediatric, cerebral vascular, cephalic (adult), cephalic (neonatal), fetal/obstetric,...

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

The hazard

The fasteners securing the control panel assembly to the base of the Philips EPIQ Ultrasound System may loosen over time, which could subsequently lead to the detachment of the entire assembly from the ultrasound system.

What to do

FDA enforcement status: Terminated

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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