Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GE Vivid E7 ultrasound system Product Usage: Vivid E7 is Recalled by GE Medical Systems Ultrasound & Primary Care Diagnostics, LL Due to The system side of the power cord may...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact GE Medical Systems Ultrasound & Primary Care Diagnostics, LL directly.
Affected Products
GE Vivid E7 ultrasound system Product Usage: Vivid E7 is a general-purpose ultrasound system, specialized for use in cardiac imaging. It is intended for use by, or under the direction of a qualified physician for ultrasound imaging and analysis of Fetal/Obstetrics; Abdominal (including renal and GYN); Pediatric; Small Organ (breast, testes, thyroid); Neonatal Cephalic; Adult Cephalic; Cardiac (adult and pediatric); Peripheral Vascular (PV); Musculo-skeletal Conventional; Musculo-skeletal Superficial; Urology (including prostate); Transesophageal; Transrectal (TR); Transvaginal (TV); and Intraoperative (abdominal, thoracic, & vascular).
Quantity: 12,426 (4,717 US; 7,709 OUS ALL PRODUCTS)
Why Was This Recalled?
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About GE Medical Systems Ultrasound & Primary Care Diagnostics, LL
GE Medical Systems Ultrasound & Primary Care Diagnostics, LL has 12 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report