GE Medical Systems Ultrasound & Primary Care Diagn Recall: GE Vivid E90 ultrasound system
GE Medical Systems Ultrasound & Primary Care Diagn Recall: GE Vivid E90 ultrasound system is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: GE Medical Systems Ultrasound & Primary Care Diagnostics, LL; Product: GE Vivid E90 ultrasound system Product Usage: Vivid E80 / E90 / E95 ultrasoun
| Recalling firm | GE Medical Systems Ultrasound & Primary Care Diagnostics, LL |
|---|---|
| Product | GE Vivid E90 ultrasound system Product Usage: Vivid E80 / E90 / E95 ultrasound system is general-purpose ultrasound systems, 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; Urology (including prostate), Transesophageal; Transrectal (TR); Transvaginal (TV); and lntra |
| Reason for recall | The system side of the power cord may break and expose the electrical conductors leading to the risk of shock. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Nationwide and Puerto Rico FOREIGN: Algeria, Antigua and Barbuda, Argentina, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belarus, Belgium, Bolivia, Plurinational State of Brazil, Brazil, Brunei Darussalam, Bulgaria, Burkina Faso, Canada, Chile, China, Colombia, Congo, The Democratic Republi |
| Recall initiated | 20180322 |
| Recall number | Z-2987-2018 |
| Category | device |
| State | WI |
| Country | United States |
$29/mo
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