---
title: "NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90, REF E NR... — FDA record Z-0128-2026 | Is It on Recall"
description: "The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces."
url: https://isitonrecall.com/recall/fda-device-z-0128-2026-nutraglide-nasal-feeding-tube-with-stylet-and-enfit-5-f-6-f-x-90-ref-e-nrt-05090-i-the-nutraglide-na/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90, REF E NRT-05090-I The NutraGlide Nasal Feeding T... — FDA record Z-0128-2026

Reported completed

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Aug 12, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90, REF E NRT-05090-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestine used for the administration of nutrition, fluids, and medications in neonatal, pediatric, and adult patients.
- **Reason**: The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
- **Classification**: Class II
- **Recalling firm**: Applied Medical Technology Inc
- **Quantity**: 390 units
- **Agency-reported status**: Completed
- **Source record identifier**: Z-0128-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0128-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Box UDI (01)00842071149666(17)280601(10)250626-382, Pouch UDI: (01)00842071149543(17)280601(10)250620-245. Box UDI (01)00842071149666(17)280601(10)250623-271, Pouch UDI: (01)00842071149543(17)280601(10)250605-340. Box UDI (01)00842071149666(17)280501(10)250612-131, Pouch UDI: (01)00842071149543(17)280501(10)250529-090, (01)00842071149543(17)280501(10)250529-091, (01)00842071149543(17)280501(10)250529-092, (01)00842071149543(17)280501(10)250529-093, (01)00842071149543(17)280501(10)250529-094, (01)00842071149543(17)280501(10)250529-095. |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

US distribution to MA and RI

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Rhode Island](https://isitonrecall.com/state/rhode-island/)

## Dates in the source

- **Report date**: Oct 15, 2025
- **Recall initiation date**: Aug 12, 2025
- **Center classification date**: Oct 9, 2025

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0128-2026%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Applied Medical Technology Inc records](https://isitonrecall.com/brand/applied-medical-technology-inc/)