AMT Mini Extension SetRecalls & reported problems across all models

We found 3 models of AMT Mini Extension Set by Applied Medical Technology, Inc. in the FDA's device registry (GUDID). Together they are named in 6 adverse event reports in the FDA's MAUDE database, received between Feb 25, 2021 and Sep 11, 2026 — classified as 1 injury, 5 malfunctions.

The most frequently reported specific device problem is “Break” (6 reports).

1 FDA recall record name at least one of these models by its device identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

AMT Mini Extension Set recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Nov 26, 2024Completed

   The extension sets subject to this recall have ENFit connections, although they should have non- ENFit connections. ENFit connectors will only fit with other ENFit-compatible devices, and will not fit with non-ENFit connectors.

   Z-0819-2025 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Most reported AMT Mini Extension Set problems

AMT Mini Extension Set models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• AMT Mini™ Extension Set E6-1222

  Tubes, Gastrointestinal (And Accessories)
  1 recall0 reports
• AMT Mini Extension Set E6-1222-ISOSAF

  Tubes, Gastrointestinal (And Accessories)
  5 reports
• AMT Mini™ Extension Set E6-1221

  Tubes, Gastrointestinal (And Accessories)
  1 report

Recent AMT Mini Extension Set adverse event reports

The 6 most recent reports across all models, in the reporter's own words as published by the FDA.

• InjurySep 11, 2026Break; Fluid/Blood Leak; Difficult to Open or Close

  I have an AMT GJet tube (18Fr, 3.5, 45 length). I am on 18hr continuous J-tube feeds. Ireceive some medications via my G-tube. I was connected to both G and J extensionswhen I started throwing up, and the tip of the G extension broke off into the tube. Icalled the interventional radiology and GI teams, who directed me to the ED. Since theG port could not be shut, I was leaking gastric contents out and developed a stomachacid burn on my hypogastric region. Over the next couple weeks, two more Gextensions broke into the port. I had another ED visit, then ultimately needed acomplete tube replacement on (b)(6) 2026 as the valve was broken (secondary to theextension breaking). I required ED & medical help to prevent further stomacomplications and infection, and to minimize risk of metabolic or hemodynamicinstability as I receive medications via my tube to prevent hypoglycemia &hypotension. I had several episodes of severe hypoglycemia due to leakage of the Gport (when pushing Glycosade) and after the tube replacement, had two episodes ofhypotension (67/37 and 74/45). I no longer have the three broken extensions as AMTrequested that I ship them back to them, so I did. The extensions are

  Patient problems: Gastritis; Hypoglycemia; Low Blood Pressure/ Hypotension; Vomiting

  MAUDE report 50732447 ↗
• MalfunctionAug 11, 2026Break

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Feeding Problem

  MAUDE report 50212873 ↗
• MalfunctionMay 21, 2026Break; No Apparent Adverse Event

  PER THE ORIGINAL REPORTER IN MEDWATCH REPORT #: MW5186451, IT WAS REPORTED THAT, "MY BABY, (B)(6), HAS AN AMT GJET TUBE. THE G CONNECTORS, (NOT THE J'S), KEEPING REPEATEDLY BREAKING AND GETTING STUCK INSIDE THE PORT. THE EXTENSION THAT KEEPS BREAKING IS CALLED 12" RIGHT ANGLE FEEDING SET WITH DUAL ENFIT Y-PORT. MY BABY IS CONSTANTLY BEING PUT TO SLEEP TO GET A NEW ONE. WE AREN'T SURE HOW OR WHY IT'S HAPPENING. WE ARE SCREWING IT IN PROPERLY (LINE IT UP WITH THE LINE AND TURN IT CLOCKWISE TO LOCK). WE ALWAYS MAKE SURE IT'S SECURE AND LOCKED IN PLACE. THE J CONNECTORS ARE DIFFERENTLY QUALITY THAN THE G'S. I BELEIVE IT'S BREAKING BECAUSE THE G CONNECTORS ARE CHEAP POOR-QUALITY PLASTIC. WE CAME ACROSS MULTIPLE POSTS WITH THIS HAPPENING AND I POSTED AS WELL. IT SEEMS LIKE MULTIPLE REPORTS HAVE BEEN MADE BUT NOTHING EVER GETS DONE ABOUT IT".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25244364 ↗
• MalfunctionMay 21, 2026Break; No Apparent Adverse Event

  PER THE ORIGINAL REPORTER IN MEDWATCH REPORT #S: MW5186468 AND MW5186469, IT WAS REPORTED THAT, "THE AMT MINI ENTERAL EXTENSION SET IS BREAKING WHILE IN THE PATIENT'S G TUBE. THE PART OF THE AMT THAT INSERTS INTO THE G TUBE IS BREAKING OFF WHILE THE CONNECTION TUBING IS BEING TAKEN OFF AND ON THE PATIENT. THIS HAS HAPPENED TWICE TO THIS SAME PATIENT WITHIN A WEEK. THIS EVENT WAS REPORTED TO THE AMT VENDOR REPRESENTATIVE".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25243758 ↗
• MalfunctionNov 5, 2025Break; Leak/Splash; No Apparent Adverse Event; Break; Leak/Splash; No Apparent Adverse Event

  PER THE ORIGINAL REPORTER IN MEDWATCH REPORT #: MW5176512, IT WAS REPORTED THAT, "THE PART OF THE EXTENSION THAT GOES INTO THE G PORT OF THE G-JET IS BREAKING OFF AND IT IS UNABLE TO BE REMOVED. WHEN THIS HAPPENS, THEY ARE UNABLE TO CLOSE THE PORT AND GASTRIC CONTENTS QUICKLY LEAK OUT. ULTIMATELY IT REQUIRES URGENT SURGICAL INTERVENTION TO REPLACE THE G-JET. DAD NOTES THAT HE WAS ABLE TO GET THE PIECE OUT ONE OF THE TIMES, BUT THE OTHER TWO TIMES REQUIRED PLACEMENT OF A NEW G-JET." ITEM DISCARDED BY MEDICAL PROVIDERS AT TIME OF INTERVENTION AND UNABLE TO RETURN. WRITER MANAGES PRODUCT COMPLAINT PLATFORM AND THIS IS THE 4TH COMPLAINT FOR THIS ITEM THIS YEAR. THIS IS THE FIRST TIME SIGNIFICANT MEDICAL INTERVENTION WAS REQUIRED TO ADDRESS THE ISSUE BUT RISK OF HARM AND BEING UNABLE TO REMOVE THE PIECES ONCE BROKEN WERE PRESENT IN 2 OF THE OTHER COMPLAINTS ENTERED AS WELL".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23479581 ↗
• MalfunctionFeb 25, 2021Break; Entrapment of Device

  PER THE ORIGINAL MEDWATCH REPORT RECEIVED WITH REFERENCE #: MW5098551: "PATIENT'S MOTHER CALLED TO SAY PORT CONNECTOR TO G PORT BROKE AND LODGED ITSELF INSIDE THE ORIFICE. ER VISIT WAS REQUIRED TO REMOVE THE BROKEN PIECE."

  Patient problems: Foreign Body In Patient

  MAUDE report 11380788 ↗

Other Applied Medical Technology, Inc. products

• NutraGlide Nasal Feeding Tube8 models · 3 reports · 9 recalls
• AMT Mini ONE Extension Set5 models · 4 reports · 1 recall
• AMT Initial Placement Dilator Set2 models · 3 reports · 1 recall
• AMT Bridle4 models · 2 reports · 1 recall
• Mini ONE Balloon Button15 models · 33 reports