--- title: "NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NR... — FDA record Z-0127-2026 | Is It on Recall" description: "The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces." url: https://isitonrecall.com/recall/fda-device-z-0127-2026-nutraglide-nasal-feeding-tube-with-stylet-and-enfit-5-f-6-f-x-55-ref-e-nrt-05055-i-the-nutraglide-na/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement # NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NRT-05055-I The NutraGlide Nasal Feeding T... — FDA record Z-0127-2026 Reported completed Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice. Source date Aug 12, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## What the record says - **Product**: NutraGlide 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 stomach or intestine used for the administration of nutrition, fluids, and medications in neonatal, pediatric, and adult patients. - **Reason**: The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces. - **Classification**: Class II - **Recalling firm**: Applied Medical Technology Inc - **Quantity**: 1780 units - **Agency-reported status**: Completed - **Source record identifier**: Z-0127-2026 [Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0127-2026%22) [What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice. ## Lot and product identifiers | Label field | Details supplied by the agency | | --- | --- | | Lot, code or applicability | Box UDI (01)00842071149628(17)280601(10)250711-237, Pouch UDI: (01)00842071149505(17)280701(10)250707-412, (01)00842071149505(17)280601(10)250701-300. Box UDI (01)00842071149628(17)280701(10)250717-425, Pouch UDI: (01)00842071149505(17)280701(10)250710-247, (01)00842071149505(17)280701(10)250710-246. Box UDI (01)00842071149628(17)280601(10)250709-162, Pouch UDI: (01)00842071149505(17)280701(10)250702-222, (01)00842071149505(17)280601(10)250627-420, (01)00842071149505(17)280701(10)250702-412. Box UDI (01)00842071149628(17)280601(10)250710-217, Pouch UDI: (01)00842071149505(17)280701(10)250702-169, (01)00842071149505(17)280701(10)250702-138, (01)00842071149505(17)280701(10)250702-220, (01)00842071149505(17)280601(10)250630-093, (01)00842071149505(17)280601(10)250630-048, (01)00842071149505(17)280601(10)250630-047, (01)00842071149505(17)280601(10)250630-046, (01)00842071149505(17)280701(10)250702-170. Box UDI (01)00842071149628(17)280601(10)250710-307, Pouch UDI: (01)00842071149505(17)280701(10)250707-457, (01)00842071149505(17)280701(10)250702-414, (01)00842071149505(17)280601(10)250701-302, (01)00842071149505(17)280601(10)250701-301, (01)00842071149505(17)280701(10)250702-137. Box UDI (01)00842071149628(17)280601(10)250620-347, Pouch UDI: (01)00842071149505(17)280601(10)250617-066, (01)00842071149505(17)280601(10)250617-067, (01)00842071149505(17)280601(10)250617-101. Box UDI (01)00842071149628(17)280601(10)250626-400, Pouch UDI: (01)00842071149505(17)280601(10)250609-364. Box UDI (01)00842071149628(17)280601(10)250618-493, Pouch UDI: (01)00842071149505(17)280601(10)250609-360, (01)00842071149505(17)280601(10)250604-076, (01)00842071149505(17)280601(10)250611-223, (01)00842071149505(17)280601(10)250612-097, (01)00842071149505(17)280601(10)250609-363, (01)00842071149505(17)280601(10)250609-362. Box UDI (01)00842071149628(17)280501(10)250612-388, Pouch UDI: (01)00842071149505(17)280601(10)250605-139, (01)00842071149505(17)280601(10)250603-078, (01)00842071149505(17)280601(10)250604-383. Box UDI (01)00842071149628(17)280601(10)250616-372, Pouch UDI: (01)00842071149505(17)280601(10)250604-075, (01)00842071149505(17)280601(10)250604-382, (01)00842071149505(17)280601(10)250605-338. | Match all identifying details in the current notice. A brand name alone is not enough. ## Distribution US distribution to MA and RI States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address. - [Massachusetts](https://isitonrecall.com/state/massachusetts/) - [Rhode Island](https://isitonrecall.com/state/rhode-island/) ## Dates in the source - **Report date**: Oct 15, 2025 - **Recall initiation date**: Aug 12, 2025 - **Center classification date**: Oct 9, 2025 FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable. ## What to do next Read the official notice for the action that applies to your exact product. [Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0127-2026%22) ## Related records [Medical devices records](https://isitonrecall.com/category/medical-devices/) [Applied Medical Technology Inc records](https://isitonrecall.com/brand/applied-medical-technology-inc/)