HIGH

Applied Medical Technology Recalls NutraGlide ENFit Nasal Feeding Tube 5F-6F x 55 in (1,780 units)

Applied Medical Technology recalled 1,780 NutraGlide ENFit nasal feeding tubes distributed in Massachusetts and Rhode Island. Distal tips on these devices may detach at lower than expected forces. Stop using immediately and follow the 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

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About This Product

NutraGlide Nasal Feeding Tubes are used to deliver nutrition, fluids, and medications via the nasal route into the stomach or intestine across neonatal, pediatric, and adult patients.

Why This Is Dangerous

The distal tip detachment could result in device malfunction or fragment retention, potentially harming patients and complicating care.

Industry Context

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

Real-World Impact

Hospitals and clinics may need to identify affected devices, halt use, and arrange replacements, potentially affecting patient care timelines and costs.

Practical Guidance

How to identify if yours is affected

  1. Locate the model number on the device label to confirm REF E NRT-05055-I
  2. Verify device size listed as 5F-6F x 55
  3. Check for lot numbers if provided on packaging or labeling
  4. Compare to recall notice to confirm coverage

Where to find product info

Recall notices and instructions are published on the FDA enforcement page and the manufacturer communications.

What timeline to expect

4-6 weeks for refunds or replacements is common, but timelines vary by provider and recall scope.

If the manufacturer is unresponsive

  • Escalate to hospital risk management and patient safety officer
  • File a complaint with FDA or CPSC as appropriate for medical devices
  • Maintain documentation of all communications with the manufacturer and clinician

How to prevent similar issues

  • Ask vendors whether devices use ENFit with secured tips
  • Check labeling for REF E NRT-05055-I before use
  • Prefer devices with detachable-tip mechanisms clearly tested for retention

Documentation advice

Keep the recall notice, device labeling, serial numbers, photos, and all correspondence with the manufacturer for records.

Product Details

Model numbers: REF E NRT-05055-I. Distribution: US distribution to MA and RI. Sold from: Unknown. Price: Unknown.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • 1780 units recalled
  • Size 5F-6F x 55
  • ENfit connector
  • Distributed to MA and RI

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

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Safety Assessment

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

Product Details

Model Numbers
REF E NRT-05055-I
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
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