---
title: "Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tub... — FDA record Z-0496-2026 | Is It on Recall"
description: "The nasal feeding tube may be occluded"
url: https://isitonrecall.com/recall/fda-device-z-0496-2026-applied-medical-technology-inc-nutraglide-5-f-6-f-x-90-nasal-feeding-tube-with-stylet-and-enfit-ref/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I — FDA record Z-0496-2026

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 Oct 6, 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**: Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I
- **Reason**: The nasal feeding tube may be occluded
- **Classification**: Class II
- **Recalling firm**: Applied Medical Technology Inc
- **Quantity**: Not supplied
- **Agency-reported status**: Completed
- **Source record identifier**: Z-0496-2026

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0496-2026%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 P/N NFT-05090-I, Lot Number 250821-238, exp. 2027-10-01, UDI (01)00842071149666(17)271001(10)250821-238, Pouch P/N ENFT-05090-I, Lot Number 250812-470, exp. 2027-11-01, UDI (01)00842071149543(17)271101(10)250812-470; Box P/N NFT-05090-I, Lot Number 250815-355, exp. 2027-10-01, UDI (01)00842071149666(17)271001(10)250815-355, Pouch P/N ENFT-05090-I, Lot Number 250812-468, exp. 2027-10-01, UDI (01)00842071149543(17)271001(10)250812-468. |

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

## Distribution

US Nationwide distribution in the states of MA, RI, NC, OH.

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

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- [Wyoming](https://isitonrecall.com/state/wyoming/)

## Dates in the source

- **Report date**: Nov 19, 2025
- **Recall initiation date**: Oct 6, 2025
- **Center classification date**: Nov 13, 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-0496-2026%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/)
