Recall Z-0498-2026— Applied Medical Technology Inc

Name: FDA recall Z-0498-2026
Creator: U.S. Food and Drug Administration
Published: 2025-10-06

Class II · Ongoing

Class II FDA medical device recall by Applied Medical Technology Inc, initiated 2025-10-06. It names one FDA 510(k) clearance: K202539. Product: Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I. Reason: The nasal feeding tube may be occluded.

Recalling firm: Applied Medical Technology Inc
Classification: Class II
Status: Ongoing
Initiated: 2025-10-06
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

Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-I

Reason for recall

The nasal feeding tube may be occluded

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