Class II U.S. Food and Drug Administration

Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 recall: The nasal feeding tube may be occluded

Recall published 11 months ago

The nasal feeding tube may be occluded

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 tube may be occluded

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-0496-2026
Published
November 19, 2025
Risk level
Class II
Status
Completed
Issued by
U.S. Food and Drug Administration
Brand
Applied Medical Technology Inc
Product type
Medical devices
Distribution
Nationwide
Made in
United States
Lot / code info
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.
UPC codes
00842071149666, 00842071149543

Products covered by this recall

Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I

Check your product

The notice names 14 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

Lot or batch code

Usually ink-stamped near the seam, the cap or the bottom of the pack.

  • 250821-238
  • exp. 2027-10-01
  • UDI
  • 250812-470
  • exp. 2027-11-01
  • 250815-355
  • 250812-468

Best-by / use-by date

Printed beside the lot code, not on the price sticker.

  • 2027-10-01
  • UDI
  • 2027-11-01

Model or item number

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

  • ENfit
  • N NFT-05090-I

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 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.

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 tube may be occluded The nasal feeding tube may be occluded

How do I know if I have the recalled product?

Match the codes printed on your package against the notice: UPC 00842071149666, 00842071149543; lot code 250821-238, exp. 2027-10-01, UDI; best-by date 2027-10-01 or UDI; model number ENfit, N NFT-05090-I. 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.

Where was the recalled product sold?

It was distributed nationwide.

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