LOGIQ eRecalls & reported problems
GE Medical Systems (China) Co.,Ltd. · LOGIQ e · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00840682103855), received between Mar 5, 2025 and Aug 4, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fire” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Fire1
- Sparking1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, 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 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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