NutraGlide Nasal Feeding Tubes with Stylet and ENFit (5F-6F x 55) recalled due to distal tips detaching at lower forces. Check UDI codes for affected units.
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Applied Medical Technology recalls certain NutraGlide Nasal Feeding Tubes because their distal tips can detach unexpectedly. This could lead to the tube becoming dislodged during use, potentially causing injury or complications for patients needing feeding assistance.
The distal tips of these feeding tubes may detach at forces lower than expected. This could cause the tube to become dislodged during use, potentially leading to complications like improper feeding or injury.
Patients using these tubes for feeding, especially neonates, children, or adults requiring medical nutrition support. Those with the specific UDI codes listed in the recall are most at risk.
Check for the UDI codes listed in the recall: Box UDI codes starting with (01)00842071149628 and Pouch UDI codes starting with (01)00842071149505. The product is a nasal feeding tube used for administering nutrition in medical patients.
Look for Box UDI codes starting with (01)00842071149628 and Pouch UDI codes starting with (01)00842071149505 on the packaging.
The distal tips may detach at lower forces than expected, which could lead to the tube becoming dislodged during use.
Check for Box UDI codes starting with (01)00842071149628 and Pouch UDI codes starting with (01)00842071149505 on the packaging.
The recall does not require immediate discontinuation; however, you should check the UDI codes to confirm if your product is affected.
We’ve drafted a message you can send Applied Medical Technology to request your refund or repair — edit it as you like.
Subject: Recall Z-0127-2026 — Applied Medical Technology Applied Medical Technology Hello, I own a Applied Medical Technology that is covered by recall Z-0127-2026 from Applied Medical Technology. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
