Solar GI HRIM Solid State, Trolley system G3-10Recalls & reported problems

Medical Measurement Systems B.V. · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports: 1
Deaths reported: 0
Injuries reported: 0
Recalls naming it: 0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08717775955108), received between Aug 11, 2026 and Aug 11, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Decrease in Pressure” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Decrease in Pressure1

Patient problems

Convulsion/Seizure1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

MalfunctionAug 11, 2026Decrease in Pressure
Patient problems: Convulsion/Seizure
MAUDE report 50214327 ↗

Device details

UDI-DI	`08717775955108`
Brand	Solar GI HRIM Solid State, Trolley system
Model	G3-10
Company	Medical Measurement Systems B.V.
Product code	FFX · SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL)
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	—
Single use	No
Sterile	No
MRI safety	Labeling does not contain MRI Safety Information
Status	In Commercial Distribution
Record updated	Jan 12, 2026

Device type (GMDN): Gastroduodenal motility analysis system

An assembly of devices designed to evaluate peristaltic motility in the stomach and/or small intestines (usually the duodenum) by measuring pressure on an intragastric catheter/probe at several points. It typically includes a monitor display, computer, software, pressure catheter/probe, and a pH electrode to measure the acidity of the stomach contents. The system is intended to evaluate several diseases of the stomach and small intestines including the prediction of gastric and/or duodenal ulcers.

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All SYSTEM, GASTROINTESTINAL MOTILITY (ELECTRICAL) devices →

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 14, 2026 · each report above links to its original FDA record
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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