NutraGlide Nasal Feeding Tube recallZ-0130-2026 · Applied Medical Technology Inc · initiated Aug 12, 2025
Completed
Is my device affected?
- 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.
- 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.
- 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 tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
FDA root cause category: Process control
What the company is doing
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.
Recall details
- Recall number
- Z-0130-2026
- Status
- Completed
- Initiated by the company
- Aug 12, 2025
- Posted by the FDA
- Oct 9, 2025
- Recalling firm
- Applied Medical Technology Inc
- Quantity
- 200 units
- Product code
- KNT
- Distribution
- US distribution to MA and RI
Product description
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 90, REF E NRT-06090-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.
Code information (models, lots, serial numbers)
Box UDI (01)00842071149161(17)280501(10)250616-082, Pouch UDI (01)00842071149086(17)280601(10)250604-073, (01)00842071149086(17)280601(10)250604-377. Box UDI (01)00842071149161(17)280601(10)250618-317, Pouch UDI (01)00842071149086(17)280601(10)250609-271, (01)00842071149086(17)280601(10)250610-219.
Devices named in this recall
1 device in the FDA device registry whose identifier appears in the recall's code information.
- NutraGlide Nasal Feeding Tube ENFT-06090-IApplied Medical Technology, Inc. · Tubes, Gastrointestinal (And Accessories)2 recalls0 reports
Product lines
Other products in the same recall event
The FDA groups related products into one recall event (event 97448).
- Z-0127-2026 · CompletedNutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NRT-05055-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the…
- Z-0128-2026 · CompletedNutraGlide 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…
- Z-0129-2026 · CompletedNutraGlide 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…
Sources and updates
- Recall record: FDA Medical Device Recalls, file dated Oct 16, 2026 · View the FDA recall notice ↗
- Devices: FDA GUDID, file dated Oct 13, 2026. Devices are linked when their identifier (with a valid check digit) appears in the recall's code information.
- Page last rebuilt: Oct 16, 2026. Text above is shown as published by the FDA.
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