Micro G-Jet® MGJ-1415-15Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842071124342), received between May 11, 2022 and May 11, 2022 — classified as 1 injury.

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

Recent adverse event reports

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

• InjuryMay 11, 2022Adverse Event Without Identified Device or Use Problem

  PER THE ORIGINAL REPORTER, A GUIDEWIRE WAS USED TO ASSIST IN THE PLACEMENT OF A MICRO GJ DEVICE. IT WAS INDICATED THAT DURING A DEVICE PLACEMENT THERE WAS SOME FORCE TO GET THE GASTRIC PORTION OF THE TUBE THROUGH THE ABDOMINAL WALL. ONCE THE TUBE PLACEMENT WAS COMPLETE, IT WAS CHECKED UNDER FLUORO AND IT WAS NOTED THAT THERE WAS A PERFORATION IN THE SMALL BOWEL. TWO SURGEONS WERE ABLE TO REPAIR THE PERFORATION AND THE GJ DEVICE REMAINED IN PLACE AND THE PATIENT RECOVERED IN THE PICU. THE REPORTER HAD INDICATED THE CAUSE OF THE PERFORATION WAS RELATED TO OTHER PATIENT CONDITIONS AND FACTORS, INCLUDING CARDIAC DISEASE AND DYSPHAGIA, AS WELL AS A PREVIOUS TYPE OF TUBE THAT WAS IN PLACE PRIOR TO THE GJ DEVICE PLACEMENT. HOWEVER, AS THE PERFORATION WAS FOUND AFTER THE PLACEMENT PROCEDURE OF THE DEVICE IN QUESTION, THIS REPORT IS BEING REPORTED TO FDA OUT OF CAUTION.

  Patient problems: Bowel Perforation

  MAUDE report 14364955 ↗