LOGIQRecalls & reported problems across all models
GE Medical Systems (China) Co.,Ltd. · 2 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names at least one LOGIQ model. Check whether yours is affected in the recall details, and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls
- 1
We found 2 models of LOGIQ by GE Medical Systems (China) Co.,Ltd. in the FDA's device registry (GUDID). Together they are named in 2 adverse event reports in the FDA's MAUDE database, received between Mar 5, 2025 and Aug 4, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fire” (1 report).
1 FDA recall record name at least one of these models by its device identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
LOGIQ recalls
FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.
- May 16, 2025Class IIOpen, Classified
GE HealthCare has become aware that the Estimated Fetal Weight (EFW) measurement data feature on the Versana Premier R3 and LOGIQ F R3 series ultrasound systems can display previous obstetric patient data in the Whizz report. This could potentially lead to an incorrect clinical decision due to inaccuracy in the fetal size and growth calculation.
Z-2029-2025 · Root cause: Software design (manufacturing process) · Recall details · FDA record ↗
Most reported LOGIQ problems
Device problems
- Fire1
- Sparking1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
LOGIQ models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- LOGIQ LOGIQ F R3System, imaging, pulsed echo, ultrasonic1 recall0 reports
- LOGIQ eSystem, imaging, pulsed echo, ultrasonic2 reports
Recent LOGIQ adverse event reports
The 2 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionAug 4, 2025Fire; Fire
IT WAS REPORTED THAT THERE WERE FLAMES FROM THE BACK OF THE SYSTEM WHERE THE POWER CONNECTOR GOES INTO THE SYSTEM. THE FLAMES STOPPED RIGHT AFTER THE UNIT WAS UNPLUGGED. THERE WAS NO NEED FOR AN EXTINGUISHER. THERE WERE NO INJURIES REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22710060 ↗MalfunctionMar 5, 2025Sparking; Sparking
IT WAS REPORTED THAT FOLLOWING A PROCEDURE IN THE OPERATING ROOM (OR) AND WHILE STAFF WAS MOVING EQUIPMENT WITHIN THE OR, THE ULTRASOUND SYSTEM WAS UNPLUGGED FROM THE WALL WHEN IT WAS NOTICED THAT THE BATTERY BEGAN TO SMOKE AND SPARK. THE ANESTHESIA TECHNOLOGIST REMOVED THE BATTERY FROM THE SYSTEM WHICH HALTED THE SPARKING. THE PATIENT WAS STILL IN THE ROOM AT THE TIME OF THE INCIDENT, BUT THE SYSTEM WAS NOT IN USE ON THE PATIENT. NO INJURIES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21522630 ↗
Other GE Medical Systems (China) Co.,Ltd. products
All GE Medical Systems (China) Co.,Ltd. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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