FDA Device recall 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 Feeding Tube is a feeding tube…
- FDA Device
- Class II
- completed
- Published 2025-10-15
On 2025-10-15 the FDA classified a Class II 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… by Applied Medical Technology, citing the nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0129-2026 |
| Classification | Class II |
| Status | completed |
| Initiated | 2025-08-12 |
| Published | 2025-10-15 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Applied Medical Technology |
| Distribution | MA, RI |
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.
Reason
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Identifiers
| code_info | Box UDI (01)00842071149123(17)280601(10)250711-319, Pouch UDI: (01)00842071149048(17)280601(10)250627-421, (01)0084207…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 U |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0129-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.