FDA Medical Device Recalls (openFDA)
Applied Medical Technology Inc: 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 administration of nutrition, fluids, and medications in neonatal, pediatric, and adult patients.
- Recall number
- Z-0127-2026
- Recalling firm
- Applied Medical Technology Inc
- Product
- 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 administration of nutrition, fluids, and medications in neonatal, pediatric, and adult patients.
- Status
- Completed
- Initiated
- 2025-08-12
- Posted
- 2025-10-09
- Terminated
- not on file
- Reason
- The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
- Root cause
- Process control
- Action
- 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.
- Quantity
- 1780 units
- Distribution
- US distribution to MA and RI
- Lot, serial or model codes
- Box UDI (01)00842071149628(17)280601(10)250711-237, Pouch UDI: (01)00842071149505(17)280701(10)250707-412, (01)00842071149505(17)280601(10)250701-300. Box UDI (01)00842071149628(17)280701(10)250717-425, Pouch UDI: (01)00842071149505(17)280701(10)250710-247, (01)00842071149505(17)280701(10)250710-246. Box UDI (01)00842071149628(17)280601(10)250709-162, Pouch UDI: (01)00842071149505(17)280701(10)250702-222, (01)00842071149505(17)280601(10)250627-420, (01)00842071149505(17)280701(10)250702-412. Box UDI (01)00842071149628(17)280601(10)250710-217, Pouch UDI: (01)00842071149505(17)280701(10)250702-169, (01)00842071149505(17)280701(10)250702-138, (01)00842071149505(17)280701(10)250702-220, (01)00842071149505(17)280601(10)250630-093, (01)00842071149505(17)280601(10)250630-048, (01)00842071149505(17)280601(10)250630-047, (01)00842071149505(17)280601(10)250630-046, (01)00842071149505(17)280701(10)250702-170. Box UDI (01)00842071149628(17)280601(10)250710-307, Pouch UDI: (01)00842071149505(17)280701(10)250707-457, (01)00842071149505(17)280701(10)250702-414, (01)00842071149505(17)280601(10)250701-302, (01)00842071149505(17)280601(10)250701-301, (01)00842071149505(17)280701(10)250702-137. Box UDI (01)00842071149628(17)280601(10)250620-347, Pouch UDI: (01)00842071149505(17)280601(10)250617-066, (01)00842071149505(17)280601(10)250617-067, (01)00842071149505(17)280601(10)250617-101. Box UDI (01)00842071149628(17)280601(10)250626-400, Pouch UDI: (01)00842071149505(17)280601(10)250609-364. Box UDI (01)00842071149628(17)280601(10)250618-493, Pouch UDI: (01)00842071149505(17)280601(10)250609-360, (01)00842071149505(17)280601(10)250604-076, (01)00842071149505(17)280601(10)250611-223, (01)00842071149505(17)280601(10)250612-097, (01)00842071149505(17)280601(10)250609-363, (01)00842071149505(17)280601(10)250609-362. Box UDI (01)00842071149628(17)280501(10)250612-388, Pouch UDI: (01)00842071149505(17)280601(10)250605-139, (01)00842071149505(17)280601(10)250603-078, (01)00842071149505(17)280601(10)250604-383. Box UDI (01)00842071149628(17)280601(10)250616-372, Pouch UDI: (01)00842071149505(17)280601(10)250604-075, (01)00842071149505(17)280601(10)250604-382, (01)00842071149505(17)280601(10)250605-338.
- 510(k) numbers
- ["K202539"]
- PMA numbers
- not on file
- Product code
- KNT
- Firm FEI
- 1526012
- Firm city
- Brecksville
- Firm state
- OH
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28