Food, drugs, devices › Applied Medical Technology Inc
Device recall: Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I
FDA enforcement event 97804 is a device recall by Applied Medical Technology Inc of Brecksville, OH, initiated 6 Oct 2025 and classified Class II, with 5 product records.
FDA defines Class II as a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote. 85% of the 945 device enforcement events initiated in 2025 carry the same class.
Status: Completed. Initiation: voluntary: firm initiated. Applied Medical Technology Inc has 8 enforcement events on this register, with a median of 2 product records per event.
Recall classification reflects the relative degree of health hazard. Text in quotation marks is FDA's. openFDA export dated 28 Sep 2026.
Recalling firm
Applied Medical Technology Inc, Brecksville, OH.
Reason for recall
"The nasal feeding tube may be occluded"
Distribution
"US Nationwide distribution in the states of MA, RI, NC, OH."
Product records
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| Z-0494-2026 | Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I | — | Class II | Completed | 19 Nov 2025 |
| Z-0495-2026 | Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-N-I | — | Class II | Completed | 19 Nov 2025 |
| Z-0496-2026 | Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I | — | Class II | Completed | 19 Nov 2025 |
| Z-0497-2026 | Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06055-I | — | Class II | Completed | 19 Nov 2025 |
| Z-0498-2026 | Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I | — | Class II | Completed | 19 Nov 2025 |
Context
Other enforcement events for Applied Medical Technology Inc
| Initiated | Product (first record) | Type | Class | Records |
|---|---|---|---|---|
| 12 Aug 2025 | NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 6 F x 55, REF E NRT-05055-I The NutraGlide Nasal Feeding Tube | Device | Class II | 4 |
| 26 Nov 2024 | AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222 | Device | Class II | 1 |
| 14 May 2024 | AMT Initial Placement Dilator Set. Used to place gastrostomy devices. | Device | Class II | 1 |
| 10 Nov 2020 | AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102. Box PN TRN102, Box UDI (01)00842071109066 | Device | Class III | 1 |
| 19 Jan 2017 | AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes. | Device | Class III | 2 |
| 17 Feb 2016 | TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY Product Usage: Indica | Device | Class II | 4 |
| 26 Jan 2016 | AMT G-Jet¿ Low-Profile Transgastric-Jejunal Feeding Device 14F 1.5cm 45cm SINGLE USE ONLY Rx ONLY STERILE. For use in pa | Device | Class II | 1 |
All 8 events for Applied Medical Technology Inc
Questions and answers
Why was this device recalled?
FDA's record gives the reason for recall as: "The nasal feeding tube may be occluded"
What does Class II mean?
FDA classifies recalls by relative degree of health hazard. Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote.
Where was the product distributed?
FDA's distribution pattern field reads: "US Nationwide distribution in the states of MA, RI, NC, OH."
Is the recall still ongoing?
FDA lists the status as Completed. "Terminated" means FDA has determined that all reasonable efforts to remove or correct the product have been made.
Where does this data come from?
openFDA enforcement reports (food, drug and device), CC0, export dated 28 Sep 2026. Text in quotation marks is FDA's. The FDA enforcement report linked above is authoritative.
Provenance
Source: openFDA device enforcement reports (CC0), export dated 28 Sep 2026; records grouped by FDA event number. The class shown for the event is the most severe class among its records. Errors in processing are corrected at the next build; see corrections.