NutraGlide Nasal Feeding Tube ENFT-08090-IRecalls & reported problems
Applied Medical Technology, Inc. · 08FR - 10 FR x 090cm NutraGlide Nasal Feeding Tube with Stylet and ENFit® (Pouched), MDR · Class 2
All models of NutraGlide Nasal Feeding Tube (8)
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 00842071138035), received between Mar 24, 2026 and Mar 24, 2026 — classified as 1 injury.
6 other recalls cover devices cleared under the same FDA submission (K202539); they may or may not involve this specific model.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
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 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K202539. One submission often covers many models, so check the product and lot details in each record.
- Z-0497-2026 · Oct 6, 2025 · CompletedApplied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06055-I
- Z-0498-2026 · Oct 6, 2025 · CompletedApplied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I
- Z-0496-2026 · Oct 6, 2025 · CompletedApplied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I
- Z-0495-2026 · Oct 6, 2025 · CompletedApplied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-N-I
- Z-0494-2026 · Oct 6, 2025 · CompletedApplied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I
- Z-0127-2026 · Aug 12, 2025 · CompletedNutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NRT-05055-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the
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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