FDAMarch 22, 2018device

GE LOGIQ 9 ultrasound system Product Usage: The device is intended for use by a qualified physician for ultrasound evaluation of Fetal; Abdominal; Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular; Musculo-skele...

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

The hazard

The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.

What to do

FDA enforcement status: Terminated

Brands named

ge medical systems ultrasound primary care diagnostics ll

Recall history

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

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