CLASS II Device recall · Reported 19 Nov 2025 · FDA Enforcement Report

NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit recalled

Applied Medical Technology is recalling NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, distributed nationwide in the US. The recall was initiated on 6 Oct 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBox P/N NFT-06090-I, Lot Number 250825-220, exp. 2028-04-01, UDI (01)00842071149161(17)280401(10)250825-220, Pouch P/N ENFT-06090-I, Lot Number 250812-459, exp. 2028-04-01, UDI (01)00842071149086(17)280401(10)250812-459; Box P/N NFT-06090-I, Lot Number 250821-277, exp. 2028-04-01, UDI (01)00842071149161(17)280401(10)250821-277, Pouch P/N ENFT-06090-I, Lot Number 250812-453, exp. 2028-04-01, UDI (01)00842071149086(17)280401(10)250812-453; Box P/N NFT-06090-I, Lot Number 250815-364, exp. 2028-04-01, UDI (01)00842071149161(17)280401(10)250815-364, Pouch P/N ENFT-06090-I, Lot Number 250812-458, exp. 2028-04-01, UDI (01)00842071149086(17)280401(10)250812-458.

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-0498-2026
FDA event ID
97804
Recalling firm
Applied Medical Technology, Brecksville, OH
Classification
Class II
Status
Completed
Recall initiated
6 Oct 2025
FDA classified
13 Nov 2025
Reported
19 Nov 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons

Timeline

6 Oct 2025Recall initiated by company
13 Nov 2025Classified by FDA+38 days
19 Nov 2025Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

The nasal feeding tube may be occluded

Product as listed by the FDA

Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I

Where it was distributed

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

Nationwide MassachusettsNorth CarolinaOhioRhode Island

Questions about this recall

Why was it recalled?

The nasal feeding tube may be occluded

Which lots are affected?

Box P/N NFT-06090-I, Lot Number 250825-220, exp. 2028-04-01, UDI (01)00842071149161(17)280401(10)250825-220, Pouch P/N ENFT-06090-I, Lot Number 250812-459, exp. 2028-04-01, UDI (01)00842071149086(17)280401(10)250812-459; Box P/N NFT-06090-I, Lot Number 250821-277, exp. 2028-04-01, UDI (01)00842071149161(17)280401(10)250821-277, Pouch P/N ENFT-06090-I, Lot Number 250812-453, exp. 2028-04-01, UDI (01)00842071149086(17)280401(10)250812-453; Box P/N NFT-06090-I, Lot Number 250815-364, exp. 2028-04-01, UDI (01)00842071149161(17)280401(10)250815-364, Pouch P/N ENFT-06090-I, Lot Number 250812-458, exp. 2028-04-01, UDI (01)00842071149086(17)280401(10)250812-458.

Where was it sold?

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

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 97804

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