Brecksville, OH, United States
Applied Medical Technology Inc recalls
5 recalls recorded since 2018, most recently on 6 October 2025. None are listed as ongoing. Status and classification are as published by the FDA.
Recalls5
Ongoing (FDA)0
Terminated or completed5
Class I (FDA)0
Completed Class II Medical devices
- Recall started
- 6 October 2025
- Reason
- The nasal feeding tube may be occluded
- Distribution
- US Nationwide distribution in the states of MA, RI, NC, OH.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-0498-2026, Z-0497-2026, Z-0496-2026, Z-0495-2026, Z-0494-2026
- Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I
- Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06055-I
- Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I
- Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-N-I
- Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-I
Completed Class II Medical devices
- Recall started
- 12 August 2025
- Reason
- The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
- Distribution
- US distribution to MA and RI
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-0129-2026, Z-0127-2026, Z-0130-2026, Z-0128-2026
- 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 placed through the nose and ending in the stomach or intestine used for the admi
- 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 admi
- NutraGlide Nasal Feeding Tube with Stylet and ENFit, 5 F - 8 F x 90, REF E NRT-06090-I The NutraGlide Nasal Feeding Tube is a feeding tube placed through the nose and ending in the stomach or intestine used for the admi
- 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 admi
Completed Class II Medical devices
- Recall started
- 26 November 2024
- Reason
- The extension sets subject to this recall have ENFit connections, although they should have non- ENFit connections. ENFit connectors will only fit with other ENFit-compatible devices, and will not fit with non-ENFit connectors.
- Distribution
- US Distribution to states of: CA, CT, FL, GA, IL, MA, MD, MO, NC, NJ, NY, OH, OK, PA, SC, TX, VA, WA
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0819-2025
- AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222
Completed Class II Medical devices
- Recall started
- 14 May 2024
- Reason
- Devices were labelled with the incorrect guidewire labelling.
- Distribution
- US Nationwide distribution in the states of GA, IL, IN, LA, NC, NE, SC, TN, TX, UT, VA, WA, & WV.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2238-2024
- AMT Initial Placement Dilator Set. Used to place gastrostomy devices.
Terminated Class III Medical devices
- Recall started
- 10 November 2020
- Terminated
- 3 September 2021
- Reason
- The products subject to this recall may contain obvious, incorrect pouch labels while the outer box has the correct label.
- Distribution
- US Nationwide distribution in the states of CA, GA, IL, MA, MO, PA, TX, VA. No foreign distribution.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-0698-2021
- AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter, Model Number ETRN102. Box PN TRN102, Box UDI (01)00842071109066(17)230901(10)200918-103, Pouch PN ETRN102, Pouch UDI (01)00842071108007(17)230901(10)200902-075
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.