Recall archive / FDA device enforcement
NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 90, REF E NRT-05090-I The NutraGlide Nasal Feeding T... — FDA record Z-0128-2026
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. Source coverage and dates.
What the record says
- Product
- NutraGlide 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 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
- 390 units
- Agency-reported status
- Completed
- Source record identifier
- Z-0128-2026
What the recall classes mean. 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)00842071149666(17)280601(10)250626-382, Pouch UDI: (01)00842071149543(17)280601(10)250620-245. Box UDI (01)00842071149666(17)280601(10)250623-271, Pouch UDI: (01)00842071149543(17)280601(10)250605-340. Box UDI (01)00842071149666(17)280501(10)250612-131, Pouch UDI: (01)00842071149543(17)280501(10)250529-090, (01)00842071149543(17)280501(10)250529-091, (01)00842071149543(17)280501(10)250529-092, (01)00842071149543(17)280501(10)250529-093, (01)00842071149543(17)280501(10)250529-094, (01)00842071149543(17)280501(10)250529-095. |
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.
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.