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
Locate the model number on the device label to confirm REF E NRT-05055-I
Verify device size listed as 5F-6F x 55
Check for lot numbers if provided on packaging or labeling
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.
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.
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 recalls NutraGlide ENFit Nasal Feeding Tubes distributed to facilities in Massachusetts and Rhode Island. The distal tips may detach at lower than expected forces. Hospitals and patients should stop using the devices and follow recall instructions.