Z-0129-2026Class II

NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55, REF E NRT-06055-I The NutraGlide Nasal...

Name: Z-0129-2026 NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55, REF E NRT-06055-I The NutraGlide Nasal...
Creator: Applied Medical Technology Inc
Published: 2025-08-12
License: https://open.fda.gov/license/

Applied Medical Technology Inc / initiated 2025-08-12 / Completed / root cause: manufacturing process

FDA source

Applied Medical Technology Inc began a recall of NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55, REF E NRT-06055-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the... on 2025-08-12. FDA classified it as Class II and gives the reason as "The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces". As of 2026-09-10, the recall status on record is Completed, and MDM tags the root cause as manufacturing process.

Recall record

Recall number: Z-0129-2026
Classification: Class II
Status: Completed
Initiated: 2025-08-12
Posted: 2025-10-09
Recalling firm: Applied Medical Technology Inc
Product: NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 55, REF E NRT-06055-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.
Product code: KNT Tubes, Gastrointestinal (And Accessories)
Reason for recall: The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Root cause tag: manufacturing process
FDA root cause: Process control
Action: AMT issued an URGENT: MEDICAL DEVICE RECALL notice to its consignees on 8/12/2025 via USPS certified mail. The notice explained the issue, risk to health and requested the following: ACTIONS TO BE TAKEN: CUSTOMER OR USER: Applied Medical Technology, Inc. requests that customers IMMEDIATELY TAKE THE FOLLOWING ACTIONS: " Examine your inventory and isolate/quarantine pending return of the product subject to this recall. " Do not use any device subject to this recall. " Complete and return to Applied Medical Technology, Inc. the enclosed RECALL NOTIFICATION ACKNOWLEDGMENT via fax or send by mail. " Please contact Applied Medical Technology, Inc. either by phone at 440-717-4000, or via email at [email protected], to make arrangements for the return of any devices related to this recall. Include the product, all of its components, and any available packaging and labeling associated with the device.
Quantity in commerce: 840 units
Distribution: US distribution to MA and RI
Product codes and lots: Box UDI (01)00842071149123(17)280601(10)250711-319, Pouch UDI: (01)00842071149048(17)280601(10)250627-421, (01)00842071149048(17)280601(10)250627-424. Box UDI (01)00842071149123(17)280601(10)250709-071, Pouch UDI: (01)00842071149048(17)280601(10)250627-422, (01)00842071149048(17)280601(10)250627-423, (01)00842071149048(17)280601(10)250627-130. Box UDI (01)00842071149123(17)280601(10)250623-205, Pouch UDI: (01)00842071149048(17)280601(10)250612-094, (01)00842071149048(17)280601(10)250617-197, (01)00842071149048(17)280601(10)250610-228. Box UDI (01)00842071149123(17)280601(10)250625-594, Pouch UDI: (01)00842071149048(17)280601(10)250623-386, (01)00842071149048(17)280601(10)250623-388, (01)00842071149048(17)280601(10)250619-426. Box UDI (01)00842071149123(17)280601(10)250626-238, Pouch UDI: (01)00842071149048(17)280601(10)250624-271, (01)00842071149048(17)280601(10)250619-353, (01)00842071149048(17)280601(10)250623-389, (01)00842071149048(17)280601(10)250619-425. Box UDI (01)00842071149123(17)280601(10)250626-342, Pouch UDI: (01)00842071149048(17)280601(10)250624-270. Box UDI (01)00842071149123(17)280601(10)250616-344, Pouch UDI: (01)00842071149048(17)280601(10)250610-229.

Enforcement reports

One row per recalled product line

FDA enforcement reports joined to recall event Z-0129-2026
Recall number	Class	Status	Voluntary or mandated	Report date	Classified
Z-0127-2026	Class II	Completed	Voluntary: Firm initiated	2025-10-15	2025-10-09
Z-0128-2026	Class II	Completed	Voluntary: Firm initiated	2025-10-15	2025-10-09
Z-0129-2026	Class II	Completed	Voluntary: Firm initiated	2025-10-15	2025-10-09
Z-0130-2026	Class II	Completed	Voluntary: Firm initiated	2025-10-15	2025-10-09

Product code KNT

The FDA recall record names no cleared device, and no clearance has been matched to it.

MDM coverage of this record lists here, newest first.

About this record

Sourced from the FDA device recall database and the FDA enforcement reports, both ingested from openFDA. The recall record supplies the product, the reason and the product code; the enforcement report supplies the classification. The two datasets are exported by FDA on different days, and the date above is the older of the two, so nothing on this page is newer than it says.

MDM adds the root cause tag, derived from FDA’s own root cause text, and the cross-links to the product code, the clearances named on the record and MDM coverage. Where a recall has not been joined to an enforcement report, no classification is shown.

Data as of 2026-09-30, the FDA export date for this dataset. Page last changed 2026-09-05. View this recall on fda.gov (opens on fda.gov)