GE Medical Systems Ultrasound & Primary Care GE Vivid E7 ultrasound system Product Usage recall — FDA Z-2990-2018
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
Overview of recall records associated with GE Medical Systems Ultrasound & Primary Care Diagnostics, LL, including dates, categories and classifications where available.
Classification mix: Class II: 8.
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
The system side of the power cord may break and expose the electrical conductors leading to the risk of shock.
This page summarizes recall records in which the official source identifies GE Medical Systems Ultrasound & Primary Care Diagnostics, LL as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.