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.
- Company
- Applied Medical Technology Inc
- Recall Initiated
- August 12, 2025
- Posted
- October 9, 2025
- Recall Number
- Z-0128-2026
- Quantity
- 390 units
- Firm Location
- Brecksville, OH
Reason for Recall
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
Lot / Code Info
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.
Root Cause
Process control
Action Taken
AMT issued an URGENT: MEDICAL DEVICE RECALL notice to its consignees on 8/12/2025 via USPS certified mail. The notice explained the issue, risk to health and requested the following: ACTIONS TO BE TAKEN: CUSTOMER OR USER: Applied Medical Technology, Inc. requests that customers IMMEDIATELY TAKE THE FOLLOWING ACTIONS: " Examine your inventory and isolate/quarantine pending return of the product subject to this recall. " Do not use any device subject to this recall. " Complete and return to Applied Medical Technology, Inc. the enclosed RECALL NOTIFICATION ACKNOWLEDGMENT via fax or send by mail. " Please contact Applied Medical Technology, Inc. either by phone at 440-717-4000, or via email at cs@appliedmedical.net, to make arrangements for the return of any devices related to this recall. Include the product, all of its components, and any available packaging and labeling associated with the device.