HIGH

Applied Medical Technology NutraGlide ENFit Nasal Feeding Tube Recall — 200 Units (2025)

Applied Medical Technology recalled 200 NutraGlide ENFit nasal feeding tubes distributed in Massachusetts and Rhode Island. The distal tips may detach at lower than expected forces. Stop using the device immediately and follow the manufacturer’s recall instructions.

Quick Facts at a Glance

Recall Date
August 12, 2025
Hazard Level
HIGH
Brand
Applied Medical Technology
Category
Health & Personal Care
Sold At
Unknown
Geographic Scope
2 states
At-Risk Groups
INFANTS, CHILDREN, GENERAL

Hazard Information

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

What You Should Do

Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact Applied Medical Technology Inc or your healthcare provider for instructions. Notification method: Letter

Get instant alerts for Health & Personal Care recalls

Be the first to know. Free instant alerts to your inbox.

No spamUnsubscribe anytime

About This Product

The NutraGlide nasal feeding tube is a medical device placed through the nose into the stomach or intestine to deliver nutrition, fluids, and medications for neonatal, pediatric, and adult patients.

Why This Is Dangerous

A distal tip detachment can occur at lower forces than expected, creating potential for patient harm during use.

Industry Context

This recall is not specified as part of a broader industry pattern.

Real-World Impact

High-risk device with potential harm to patients; hospitals and caregivers should review inventory and follow recall instructions promptly.

Practical Guidance

How to identify if yours is affected

  1. Identify model REF E NRT-06090-I on the device label.
  2. Review Box/Pouch UDIs: (01)00842071149161(17)280501(10)250616-082, (01)00842071149086(17)280601(10)250604-073, (01)00842071149086(17)280601(10)250604-377, (01)00842071149161(17)280601(10)250618-317, (01)00842071149086(17)280601(10)250609-271, (01)00842071149086(17)280601(10)250610-219.
  3. Check if the device is listed in the FDA recall page using the recall number Z-0130-2026.

Where to find product info

Packaging labels show the model and UDIs. The FDA recall page linked in the notice provides official guidance and instructions.

What timeline to expect

Refunds or replacements are typically processed within 4-6 weeks after the manufacturer completes the recall. Specific timelines will be provided in a

If the manufacturer is unresponsive

  • Document all communications with the manufacturer
  • Escalate to the hospital's risk management or patient safety office
  • File a consumer complaint with the FDA if necessary
  • Consult legal counsel if needed

How to prevent similar issues

  • Verify ENFit compliance when purchasing feeding tubes.
  • Check UDIs and model numbers before use.
  • Monitor for recall notices from manufacturers and FDA.
  • Purchase from reputable suppliers and hospital catalogues.
  • documentationAdvice ツ keep the recall letter, product packaging, photos, and correspondence

Documentation advice

Keep the recall notice and any communications. Photograph the device label and UDIs. Save purchase records and the replacement process message.

Product Details

Model numbers: REF E NRT-06090-I; Box UDI (01)00842071149161(17)280501(10)250616-082; Pouch UDI (01)00842071149086(17)280601(10)250604-073; (01)00842071149086(17)280601(10)250604-377; Box UDI (01)00842071149161(17)280601(10)250618-317; Pouch UDI (01)00842071149086(17)280601(10)250609-271; (01)00842071149086(17)280601(10)250610-219.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • 200 units recalled
  • Distribution to MA and RI
  • Distal-tip detachment risk
  • Model REF E NRT-06090-I and multiple UDIs listed

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

Get Alerts for Health & Personal Care Recalls

Get instant alerts for recalls that affect you. Free forever.

Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
INFANTSCHILDRENGENERAL
Injury Types
SUFFOCATIONLACERATIONOTHER

Product Details

Model Numbers
REF E NRT-06090-I
Box UDI (01)00842071149161(17)280501(10)250616-082
Pouch UDI (01)00842071149086(17)280601(10)250604-073
(01)00842071149086(17)280601(10)250604-377
Box UDI (01)00842071149161(17)280601(10)250618-317
+2 more
Affected States
MA, RI
Report Date
October 15, 2025
Recall Status
ACTIVE

Related Recalls

Health & Personal Care
HIGH

Applied Medical Technology NutraGlide ENFit Nasal Feeding Tube Recall 840 Units (2025)

Applied Medical Technology recalled 840 NutraGlide ENFit nasal feeding tubes distributed in the United States to Massachusetts and Rhode Island. The tubes have distal tips that may detach at lower than expected forces. Healthcare providers and patients should stop using the device immediately and follow the recall instructions.

Applied Medical Technology
The nasal
Read more