GE Medical Systems Ultrasound & Primary Care Diagnostics, LL recalls GE LOGIQ E9 ultrasound system Product Usage: The device
Recalled Product
GE LOGIQ E9 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-skeletal Conventional and Superficial; Urology (including prostate); Transrectal; Transvaginal; Transesophageal and Intraoperative (abdominal, thoracic and vascular).
Hazard / Issue
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
Issued by
FDA
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