Class II U.S. Food and Drug Administration

Applied Medical Technology Inc NutraGlide recall: The nasal feeding tubes, NutraGlide, subject to this recall have distal tips

Recall published 1+ years ago

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

The hazard: Device safety concern

The manufacturer or the FDA identified a problem with this device. The model, lot and catalogue numbers are what define the scope.

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

Why it matters: The FDA recorded an enforcement action against this device. Most device recalls are corrections rather than removals, so the device often stays in use while the manufacturer issues a fix.

Recall details

Recall number
Z-0130-2026
Published
October 15, 2025
Risk level
Class II
Status
Completed
Issued by
U.S. Food and Drug Administration
Brand
Applied Medical Technology Inc
Product type
Medical devices
Units affected
200 units
Distribution
Massachusetts, Rhode Island
Made in
United States
Lot / code info
Box UDI (01)00842071149161(17)280501(10)250616-082, Pouch UDI (01)00842071149086(17)280601(10)250604-073, (01)00842071149086(17)280601(10)250604-377. Box UDI (01)00842071149161(17)280601(10)250618-317, Pouch UDI (01)00842071149086(17)280601(10)250609-271, (01)00842071149086(17)280601(10)250610-219.
UPC codes
00842071149161, 00842071149086

Products covered by this recall

NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 90, REF E NRT-06090-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.

Check your product

The notice names 3 codes you can read straight off the package. Type the one printed on yours and the list below narrows to it.

UPC / barcode

Read the twelve digits under the barcode on the package.

  • 00842071149161
  • 00842071149086

Model or item number

On the rating label, the box or the instruction sheet.

  • ENFit

Codes are lifted verbatim from the FDA — Device enforcement notice. A code that is missing here may still be covered — the official notice is the complete list.

What to do about Device

Applied Medical Technology Inc — The manufacturer or the FDA identified a problem with this device. The model, lot and catalogue numbers are what define the scope.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. If the device is implanted or you depend on it daily, speak to your clinician before changing how you use it.
  3. Ask the supplier or clinic that provided it what the remedy is in your case.
  4. If you are a facility, quarantine affected stock and log the correction.

Who pays for a device recall

The manufacturer funds the remedy. The practical question is usually which link in the chain executes it.

  • If a clinic fitted or supplied the device, start there — they hold the serial-number records the manufacturer needs.
  • Ask for written confirmation that the remedy was applied to your serial number. That is what an insurer or a future clinician will want to see.
  • If you bought it yourself online or from a pharmacy, go to the manufacturer’s recall page rather than the retailer; device claims are handled centrally.
  • Where the remedy is a software update, there is nothing to claim, but do confirm the version changed afterwards.

Company contact: Applied Medical Technology Inc — 8006 Katherine Blvd, Brecksville, OH, 44141-4202

The official notice

This page summarises a notice published by U.S. Food and Drug Administration. The agency notice is the authoritative version — read it before you act, and treat it as the final word if anything here looks different.

Open the FDA — Device enforcement record U.S. Food and Drug Administration recalls

Questions people ask about this recall

Why was Applied Medical Technology Inc medical devices recalled?

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

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 00842071149161, 00842071149086; model number ENFit. If the code on your package is not on that list, your unit is outside the recall.

What should I do with it right now?

Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.

Can I get my money back?

If a clinic fitted or supplied the device, start there — they hold the serial-number records the manufacturer needs.

Which states were affected?

The notice lists Massachusetts, Rhode Island.

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