Applied Medical Technology recalls NutraGlide Nasal Feeding Tubes with risk of distal tip detachment. Affected units have specific UDI codes. Consumers should contact for remedy details.
The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.
Applied Medical Technology recalls NutraGlide Nasal Feeding Tubes that may detach at lower forces than expected. This could lead to dislodgement of the tube, causing injury or complications during medical feeding.
The distal tips of these feeding tubes can detach at lower forces than expected. This detachment could cause the tube to become dislodged, potentially leading to injury or complications during medical feeding.
Patients using NutraGlide Nasal Feeding Tubes for medical nutrition, fluids, or medications are affected. Those with specific UDI codes listed in the recall are most at risk.
Check for the UDI codes listed in the recall: Box UDI (01)00842071149161(17)280501(10)250616-082 or Pouch UDI (01)00842071149086(17)280601(10)250604-073.
Look for the specific UDI codes listed in the recall on the product packaging.
The distal tips of these feeding tubes may detach at lower forces than expected, which could lead to dislodgement and injury.
Box UDI (01)00842071149161(17)280501(10)250616-082 or Pouch UDI (01)00842071149086(17)280601(10)250604-073.
The recall does not require immediate stop use; however, affected units should be checked for the UDI codes and contacted for remedy details.
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-0130-2026 — Applied Medical Technology Applied Medical Technology Hello, I own a Applied Medical Technology that is covered by recall Z-0130-2026 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.
