NutraGlide Nasal Feeding TubeRecalls & reported problems across all models

We found 8 models of NutraGlide Nasal Feeding Tube by Applied Medical Technology, Inc. in the FDA's device registry (GUDID). Together they are named in 3 adverse event reports in the FDA's MAUDE database, received between Jun 19, 2025 and May 5, 2026 — classified as 2 injuries, 1 malfunction.

9 FDA recall records 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

NutraGlide Nasal Feeding Tube 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. Oct 6, 2025Class IICompleted

   The nasal feeding tube may be occluded

   Z-0498-2026 · Root cause: Process control · Recall details · FDA record ↗

2. Oct 6, 2025Class IICompleted

   The nasal feeding tube may be occluded

   Z-0497-2026 · Root cause: Process control · Recall details · FDA record ↗

3. Oct 6, 2025Class IICompleted

   The nasal feeding tube may be occluded

   Z-0496-2026 · Root cause: Process control · Recall details · FDA record ↗

4. Oct 6, 2025Class IICompleted

   The nasal feeding tube may be occluded

   Z-0495-2026 · Root cause: Process control · Recall details · FDA record ↗

5. Oct 6, 2025Class IICompleted

   The nasal feeding tube may be occluded

   Z-0494-2026 · Root cause: Process control · Recall details · FDA record ↗

6. Aug 12, 2025Class IICompleted

   The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

   Z-0130-2026 · Root cause: Process control · Recall details · FDA record ↗

7. Aug 12, 2025Class IICompleted

   The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

   Z-0129-2026 · Root cause: Process control · Recall details · FDA record ↗

8. Aug 12, 2025Class IICompleted

   The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

   Z-0128-2026 · Root cause: Process control · Recall details · FDA record ↗

9. Aug 12, 2025Class IICompleted

   The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

   Z-0127-2026 · Root cause: Process control · Recall details · FDA record ↗

Most reported NutraGlide Nasal Feeding Tube problems

NutraGlide Nasal Feeding Tube models

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

• NutraGlide Nasal Feeding Tube ENFT-06055-I

  Tubes, Gastrointestinal (And Accessories)
  2 recalls0 reports
• NutraGlide Nasal Feeding Tube ENFT-06090-I

  Tubes, Gastrointestinal (And Accessories)
  2 recalls0 reports
• NutraGlide Nasal Feeding Tube ENFT-05055-I

  Tubes, Gastrointestinal (And Accessories)
  2 recalls0 reports
• NutraGlide Nasal Feeding Tube ENFT-05090-I

  Tubes, Gastrointestinal (And Accessories)
  2 recalls0 reports
• NutraGlide Nasal Feeding Tube ENFT-05055-N-I

  Tubes, Gastrointestinal (And Accessories)
  1 recall0 reports
• NutraGlide Nasal Feeding Tube ENFT-05090-I

  Tubes, Gastrointestinal (And Accessories)
  1 report
• NutraGlide Nasal Feeding Tube ENFT-08090-I

  Tubes, Gastrointestinal (And Accessories)
  1 report
• NutraGlide Nasal Feeding Tube ENFT-08110-I

  Tubes, Gastrointestinal (And Accessories)
  1 report

Recent NutraGlide Nasal Feeding Tube adverse event reports

The 3 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionMay 5, 2026No Apparent Adverse Event

  PER THE ORIGINAL REPORTER IN MEDWATCH REPORT #: MW5184947, IT WAS REPORTED THAT THE "GUIDEWIRE PERFORATED DHT DURING PLACEMENT RESULTING IN THE GUIDEWIRE EXTENDING OUT THE SIDE OF THE DHT AND INTO THE STOMACH".

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25080316 ↗
• InjuryMar 24, 2026Adverse Event Without Identified Device or Use Problem

  PER INFORMATION REPORTED BY THE USER FACILITY TO AMT SALES REPRESENTATIVES, A GASTRIC PERFORATION OCCURRED ROUGHLY A MONTH AFTER THE PLACEMENT OF A NFT-08090-I. THE PERFORATION REPORTEDLY OCCURRED IN AN 11-MONTH-OLD 11KG BABY WITH LEUKEMIA. PER THE HOSPITAL'S POLICY, THIS SIZE NUTRAGLIDE WAS TOO LARGE FOR THE PATIENT, AND THEY SHOULD HAVE PLACED A 6-8F NUTRAGLIDE. IT WAS ALSO REPORTED THAT THE PATIENT HAD AN INTERNAL SAFETY REPORT THE WEEK BEFORE THE INCIDENT OCCURRED. THE HOSPITAL STAFF REPORTEDLY DID NOT KNOW HOW FAR THE TUBE WAS INSERTED AND IF IT WAS IN THE CORRECT SPOT. A PH CHECK WAS PERFORMED TO CHECK PLACEMENT. DURING THIS CHECK THE STAFF NOTED THE TUBE WAS TOO LARGE FOR THE PATIENT PER THEIR POLICY. IT WAS REPORTED THEY DECIDED TO LEAVE THE TUBE IN PLACE. DUE TO THE PERFORATION THE PATIENT WAS TAKEN TO THE OPERATING ROOM FOR URGENT REPAIR. IT WAS REPORTED TO AMT THAT THE PATIENT WAS RECOVERING FROM THE EVENT.

  Patient problems: Perforation

  MAUDE report 24673211 ↗
• InjuryJun 19, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  PER THE ORIGINAL REPORTER IN UF #: (B)(4), IT WAS REPORTED THAT A,"5 FRENCH 90CM NUTRAGLIDE NJT [NASOJEJUNAL TUBE] PLACED ON [REDACTED] FOR NUTRITION. THE PLACEMENT OF THIS TUBE WAS CONFIRMED BY X-RAY AND INSERTION WAS DONE PER HOSPITAL POLICY. ON [REDACTED], ABOUT THREE DAYS LATER, ABDOMINAL ULTRASOUND IDENTIFIED FREE FLUID NOTED IN ABDOMEN, GIVEN HCT [HEMATOCRIT] DROP, CONCERN FOR HEMOPERITONEUM. PATIENT TRANSFERRED EMERGENTLY TO ICU [INTENSIVE CARE UNIT], INTUBATED AND GEN SURGERY EXPLORATORY LAP IDENTIFIED FEEDS PRESENT IN INTRA-ABDOMINAL SPACE AND NJT FOUND TO HAVE GONE THROUGH INTESTINAL WALL ABOUT 1 CM AT THE D2-D3 JUNCTION RIGHT AS THE DUODENUM MAKES ITS TURN. INTESTINES ALL LOOKED HEALTHY, AND NO BOWEL HAD TO BE RESECTED. HOLE WAS SEWN SHUT AND ABDOMEN CLOSED".

  Patient problems: Bowel Perforation

  MAUDE report 22293496 ↗

Other Applied Medical Technology, Inc. products

• AMT Mini Extension Set3 models · 6 reports · 1 recall
• 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