FDA Device recall Z-0494-2026
Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I
- FDA Device
- Class II
- completed
- Published 2025-11-19
On 2025-11-19 the FDA classified a Class II recall of Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I by Applied Medical Technology, citing the nasal feeding tube may be occluded.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0494-2026 |
| Classification | Class II |
| Status | completed |
| Initiated | 2025-10-06 |
| Published | 2025-11-19 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Applied Medical Technology |
| Distribution | US |
Product
Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I
Reason
The nasal feeding tube may be occluded
Identifiers
| code_info | Box P/N NFT-05055-I, Lot Number 250905-220, exp. 2027-03-01, UDI (01)00842071149628(17)270301(10)250905-220, Pouch P/N…Box P/N NFT-05055-I, Lot Number 250905-220, exp. 2027-03-01, UDI (01)00842071149628(17)270301(10)250905-220, Pouch P/N ENFT-05055-I, Lot Number 250826-272, exp. 2027-03-01, UDI (01)00842071149505(17)270301(10)250826-272; Box P/N NFT-05055-I, Lot Number 250903-181, exp. 2028-01-01, UDI (01)00842071149628(17)280101(10)250903-181, Pouch P/N ENFT-05055-I, Lot Number 250826-269, exp. 2028-05-01, UDI (01)00842071149505(17)280501(10)250826-269; Box P/N NFT-05055-I, Lot Number 250829-265, exp. 2027-11-01, UDI (01)00842071149628(17)271101(10)250829-265, Pouch P/N ENFT-05055-I, Lot Number 250825-151, exp. 2027-11-01, UDI (01)00842071149505(17)271101(10)250825-151; Box P/N NFT-05055-I, Lot Number 250828-270, exp. 2027-04-01, UDI (01)00842071149628(17)270401(10)250828-270, Pouch P/N ENFT-05055-I, Lot Number 250820-454, exp. 2027-08-01, UDI (01)00842071149505(17)270801(10)250820-454; Box P/N NFT-05055-I, Lot Number 250826-394, exp. 2027-03-01, UDI (01)00842071149628(17)270301(10)250826-394, Pou |
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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-0494-2026%22
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