Micro G-Jet® MGJ-1417-30-IRecalls & reported problems
Applied Medical Technology, Inc. · 14FR x 1.7 cm x 30 cm - AMT micro G-Jet® Low Profile Transgastric-Jejunal Feeding Device (ENFit®) · Class 2 · Implant
Data updated Oct 18, 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 00842071124885), received between Jan 26, 2024 and Mar 22, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Increase in Pressure” (2 reports).
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
Most reported problems
Device problems
- Increase in Pressure2
- Material Rupture1
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Vomiting1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 22, 2024Increase in Pressure; Material Rupture; Increase in Pressure; Material Rupture
PER THE ORIGINAL REPORTER IN UF #: (B)(4), IT WAS REPORTED THAT AN "AMT MICRO G-JET 1.7CM X 30CM GJ TUBE CLOGGED AND WHEN FAMILY TRIED TO USE TUBE, TUBE BROKE ABOVE BALLOON CREATING A HOLE. PATIENT CAME IN AND TUBE WAS EXCHANGED". NO HARM WAS REPORTED TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18961701 ↗MalfunctionJan 26, 2024Increase in Pressure; Material Separation; Increase in Pressure; Material Separation
THE REPORTER INDICATED THAT "THE TUBE WAS CLOGGED AND MOM WAS FLUSHING WATER USING A SYRINGE. SHE FELT IT UNCLOG, BUT LATER THAT NIGHT THE PATIENT VOMITED UP THE BLUE TUBE PORTION OF THE GJ (JEJUNAL TUBING). THE BALLOON WAS STILL INTACT". NO HARM WAS REPORTED TO THE PATIENT.
Patient problems: Vomiting
MAUDE report 18589940 ↗
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- 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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