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RecallWatchMedical Device Safety
Class IICompletedZ-0496-2026

Applied Medical Technology Inc recalls Applied Medical Technology

Applied Medical Technology IncBrecksville, OH, United StatesReported Nov 19, 2025 · 8 months ago
Legal News Analyst ·

Reason for recall

The nasal feeding tube may be occluded

Affected product

Check your device

Enter a lot, serial, REF, or UDI number from your device's label to check it against this recall's listed codes.

Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-I

Lot / code information

Lot #
250821-238, exp. 2027-10-01
UDI
(01)00842071149666(17)271001(10)250821-238, Pouch P/N ENFT-05090-I
Lot #
250812-470, exp. 2027-11-01
UDI
(01)00842071149543(17)271101(10)250812-470; Box P/N NFT-05090-I
Lot #
250815-355, exp. 2027-10-01
UDI
(01)00842071149666(17)271001(10)250815-355, Pouch P/N ENFT-05090-I
Lot #
250812-468, exp. 2027-10-01
UDI
(01)00842071149543(17)271001(10)250812-468

What the firm is doing

Applied Medical Technology, Inc. issued an URGENT: MEDICAL DEVICE RECALL notice to its consignees on 10/06/2025 via certified mail. The notice explained the issue, potential risk to health, and requested the consignee quarantine the affected product, complete and return the acknowledgement, and contact Applied Medical Technology, Inc. either by telephone at 440-717-4000 or via email at cs@appliedmedical.net to arrange for the return of the affected product. Those who further distributed the product were directed to notify those to whom the product was transferred of this recall. For questions or concerns, contact: Customer Service, 440-717-4000 (tel), 440-717-4200 (fax), cs@appliedmedical.net (email). Hours of operation 8:30 A - 5:00 P, Eastern time

DistributionShow details

US Nationwide distribution in the states of MA, RI, NC, OH.

Class IIWhat this means

Use of the product may cause temporary or medically reversible adverse health consequences.

Sources & references

Taylor Coteus
Legal News Analyst

Taylor Coteus is RecallWatch's Legal News Analyst, covering FDA medical-device enforcement and patient-safety litigation. He reviews every recall against the FDA's official openFDA record before it is published and is responsible for corrections and editorial accuracy.

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