General Electric Med Systems LLC LOGIQ 5 system models 2331752, 2331753, 2332750, 2353313 and 2355477. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
LOGIQ 5 system models 2331752, 2331753, 2332750, 2353313 and 2355477.
Brand
General Electric Med Systems LLC
Lot Codes / Batch Numbers
all serial numbers
Products Sold
all serial numbers
General Electric Med Systems LLC is recalling LOGIQ 5 system models 2331752, 2331753, 2332750, 2353313 and 2355477. due to The Estimated Fetal Weight (EFW) result will be incorrect if the operator fails to perform the 'end exam' or new patient registration step before star. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Estimated Fetal Weight (EFW) result will be incorrect if the operator fails to perform the 'end exam' or new patient registration step before starting an EFW measurement procedure on the next patient.
Recommended Action
Per FDA guidance
Devices will have software upgrades done by GE Field Service Technicians. The upgrade will include a dialog box which will display on the screen when prior data exists and a new patient is being registered.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026