Recall Z-0127-2026— Applied Medical Technology Inc

Name: FDA recall Z-0127-2026
Creator: U.S. Food and Drug Administration
Published: 2025-08-12

Class II · Ongoing

Class II FDA medical device recall by Applied Medical Technology Inc, initiated 2025-08-12. It names one FDA 510(k) clearance: K202539. 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.. Reason: The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces..

Recalling firm: Applied Medical Technology Inc
Classification: Class II
Status: Ongoing
Initiated: 2025-08-12
Firm location: Brecksville, OH, United States

510(k) clearances named in this recall

1 on FDA's record

K202539 — Nutriglide(TM) Nasal Feeding TubeApplied Medical Technology, Inc.·cleared 2020-10-29

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

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.

Reason for recall

The nasal feeding tubes, NutraGlide, subject to this recall have distal tips that may detach at lower than expected forces.

Data sourced from openFDA. This site is unofficial and independent of the FDA.