RecallRadar

FDA Device recall Z-2983-2018

GE LOGIQ E9 ultrasound system Product Usage: The device is intended for use by a qualified physician for ultrasound evaluation of Fetal

On 2018-09-12 the FDA classified a Class II recall of GE LOGIQ E9 ultrasound system Product Usage: The device is intended for use by a qualified physician for ultrasound evaluation of Fetal by Ge Medical Systems Ultrasound And Primary Care Diagnostics Ll, citing the system side of the power cord may break and expose the electrical conductors leading to the risk of shock.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2983-2018
ClassificationClass II
Statusterminated
Initiated2018-03-22
Published2018-09-12
Last updated2026-09-13 11:54 UTC
CompanyGe Medical Systems Ultrasound And Primary Care Diagnostics Ll
DistributionUS

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).

Reason

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

Identifiers

code_infoEach consignee have one serial numbers assigned

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2983-2018%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.