Applied Medical Technology recalls NutraGlide Nasal Feeding Tubes with Stylet and ENFit (5F-6F x 90) due to risk of distal tips detaching at lower forces than expected. Affected units have specific UDI codes.
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Applied Medical Technology is recalling NutraGlide Nasal Feeding Tubes that may detach at lower forces than expected. This could cause the tube to become dislodged during use, potentially leading to complications for patients receiving nutrition or medications through the tube.
The distal tips of these feeding tubes can detach at forces lower than expected. This detachment could cause the tube to become dislodged during use, potentially leading to complications such as improper nutrition delivery or injury.
Patients using NutraGlide Nasal Feeding Tubes for nutrition or medication administration in neonatal, pediatric, or adult care are most at risk. Healthcare providers and caregivers who use these tubes should check for the recalled model.
Check for the product name 'NutraGlide Nasal Feeding Tube with Stylet and ENFit' (5F-6F x 90). Affected units have specific UDI codes listed in the recall notice.
Look for the UDI codes listed in the recall notice to confirm if your tube is affected.
The distal tips may detach at lower forces than expected, which could cause the tube to become dislodged during use.
Check for the UDI codes listed in the recall notice: Box UDI (01)00842071149666(17)280601(10)250626-382 or similar codes.
The recall does not specify a remedy, so contact the manufacturer for guidance on next steps.
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-0128-2026 — Applied Medical Technology Applied Medical Technology Hello, I own a Applied Medical Technology that is covered by recall Z-0128-2026 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.
