Micro G-Jet® MGJ-1412-10Recalls & reported problems
Applied Medical Technology, Inc. · 14FR x 1.2 cm x 10 cm - AMT micro G-Jet® Low Profile Transgastric-Jejunal Feeding Device · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842071124298), received between Jul 24, 2023 and Jul 24, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (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.
Most reported problems
Device problems
- Material Split, Cut or Torn1
Patient problems
- Aspiration Pneumonitis1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 24, 2023Material Split, Cut or Torn; Material Split, Cut or Torn
REPORTER INDICATED THAT WITHIN 7 DAYS OF PLACEMENT, THE PATIENT RETURNED TO THE HOSPITAL TO HAVE THE GJ DEVICE CHECKED DUE TO SEVERAL VOMITING EVENTS. X-RAY IMAGING WAS PERFORMED FOR SURVEILLANCE WITH POSSIBLE ASPIRATION NOTED. AN INSPECTION OF THE DEVICE FOUND THAT THE JEJUNAL SECTION OF THE TUBING HAD TORN AT AN UNKNOWN DATE, ALLOWING FEED INTENDED FOR THE JEJUNUM TO FLOW INTO THE STOMACH. THE TUBE WAS STILL PARTIALLY ATTACHED AND WAS ABLE TO BE REMOVED IN FULL. FURTHER CONVERSATION WITH NURSE DETERMINED THAT PATIENT WAS ADMITTED FOR PNEUMONIA SEVERAL DAYS LATER, THOUGH IT WAS UNKNOWN IF THE CAUSE WAS RELATED TO THE DEVICE FAILURE.
Patient problems: Aspiration Pneumonitis
MAUDE report 17376060 ↗
Other Tubes, Gastrointestinal (And Accessories) devices
- Bard® DigniShield® Stool Management System SMS002C. R. Bard, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)2 deaths525 reports
- CORTRAK* 2 ENTERAL ACCESS SYSTEM 20-0950Avanos Medical, Inc. · Tubes, gastrointestinal (and accessories)1 recall22 deaths134 reports
- Bard Tri-Funnel Replacement Gastrostomy Tube 000720Bard Access Systems, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 death170 reports
- EndoVive Safety PEG Kit M00566470Boston Scientific Corporation · TUBES, GASTROINTESTINAL (AND ACCESSORIES)1 recall1 death111 reports
- Kangaroo 8884711253Cardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)152 reports
- NutraGlide Nasal Feeding Tube ENFT-06090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- NutraGlide Nasal Feeding Tube ENFT-05090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
- Kangaroo 8884711253ECardinal Health, Inc. · TUBES, GASTROINTESTINAL (AND ACCESSORIES)100 reports
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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