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NutraGlide Nasal Feeding Tube recallZ-0495-2026 · Applied Medical Technology Inc · initiated Oct 6, 2025

Completed

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Applied Medical Technology Inc or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

The nasal feeding tube may be occluded

FDA root cause category: Process control

What the company is doing

Applied Medical Technology, Inc. issued an URGENT: MEDICAL DEVICE RECALL notice to its consignees on 10/06/2025 via certified mail. The notice explained the issue, potential risk to health, and requested the consignee quarantine the affected product, complete and return the acknowledgement, and contact Applied Medical Technology, Inc. either by telephone at 440-717-4000 or via email at [email protected] to arrange for the return of the affected product. Those who further distributed the product were directed to notify those to whom the product was transferred of this recall. For questions or concerns, contact: Customer Service, 440-717-4000 (tel), 440-717-4200 (fax), [email protected] (email). Hours of operation 8:30 A - 5:00 P, Eastern time

Recall details

Recall number
Z-0495-2026
Status
Completed
Initiated by the company
Oct 6, 2025
Posted by the FDA
Nov 13, 2025
Recalling firm
Applied Medical Technology Inc
Product code
KNT
FDA submissions
K202539
Distribution
US Nationwide distribution in the states of MA, RI, NC, OH.

Product description

Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-N-I

Code information (models, lots, serial numbers)

Box P/N NFT-05055-N-I, Lot Number 250903-152, exp. 2028-08-01, UDI (01)00842071149642(17)280801(10)250903-152, Pouch P/N ENFT-05055-N-I, Lot Number 250829-039, exp. 2028-08-01, (01)00842071149529(17)280801(10)250829-039

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

Product lines

Other devices under the same FDA submission

7 devices cleared under K202539 are not named by identifier in this recall. One submission often covers many models, so they may or may not be affected.

Other products in the same recall event

The FDA groups related products into one recall event (event 97804).

Sources and updates

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