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

This is a device enforcement record. Check whether the remedy is a correction, a software update or a removal before changing anything.

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-0128-2026
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
390 units
Distribution
Massachusetts, Rhode Island
Made in
United States
Lot / code info
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.
UPC codes
00842071149666, 00842071149543

Products covered by this recall

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.

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.

  • 00842071149666
  • 00842071149543

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 — This is a device enforcement record. Check whether the remedy is a correction, a software update or a removal before changing anything.

  1. Match the model, catalogue, lot and serial numbers on your device against the identifiers on this page.
  2. If you are a facility, quarantine affected stock and log the correction.
  3. Report device problems to the FDA through MedWatch.
  4. If the device is implanted or you depend on it daily, speak to your clinician before changing how you use it.

Replacements, repairs and reimbursement

Device remedies run through the supply chain, so the route depends on who sold you the unit.

  • Contact the distributor or clinic named on your paperwork and quote the recall number on this page. They will tell you whether the remedy is a repair, a replacement or an instruction update.
  • If the device was billed to insurance or Medicare, the replacement is usually billed the same way; you should not face a second deductible for a recall.
  • Keep every piece of correspondence. If a recalled device caused harm, that paper trail is what a claim rests on.
  • Consumer-purchased devices such as monitors and test kits are normally replaced free, with return shipping paid.

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 00842071149666, 00842071149543; 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?

Contact the distributor or clinic named on your paperwork and quote the recall number on this page. They will tell you whether the remedy is a repair, a replacement or an instruction update.

Which states were affected?

The notice lists Massachusetts, Rhode Island.

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