Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-2989-2018 — GE Vivid 7 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 G

U.S. FDA — Device Enforcement · United States · 2018-03-22 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2989-2018
Date of alert: 2018-03-22
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: GE Medical Systems Ultrasound & Primary Care Diagnostics, LL
Product category: device
Product type: Devices

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

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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