HIGH

Applied Medical Technology Recalls NutraGlide Nasal Feeding Tubes Due to Detachment Risk

Applied Medical Technology recalled 200 NutraGlide Nasal Feeding Tubes on August 12, 2025. The distal tips may detach under lower than expected forces, posing a risk to patients. This recall affects devices distributed in Massachusetts and Rhode Island.

Quick Facts at a Glance

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

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

Product Details

The recalled NutraGlide Nasal Feeding Tube models include REF E NRT-06090-I. Each tube measures 5 F - 8 F x 90 cm. The devices were distributed in the U.S. and sold to healthcare facilities.

The Hazard

The distal tips of the NutraGlide Nasal Feeding Tubes may detach during use. This detachment can lead to complications in patients requiring the feeding tubes.

Reported Incidents

No specific incidents or injuries have been reported related to this recall. The hazard level is classified as high due to the potential for serious complications.

What to Do

Stop using the recalled nasal feeding tubes immediately. Contact Applied Medical Technology or your healthcare provider for further instructions and return options.

Contact Information

For more information, contact Applied Medical Technology at 1-800-XXX-XXXX or visit their website at www.appliedmedical.com.

Key Facts

  • 200 units recalled
  • Distributed in Massachusetts and Rhode Island
  • Risk of distal tips detaching
  • Stop using immediately
  • Contact manufacturer for instructions
View Original Recall on FDA - Medical Devices

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERALCHILDRENINFANTS
Injury Types
OTHER

Product Classification

Product TypeNasal Feeding Tube
Sold At
Multiple Retailers

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
Source Agency
FDA - Medical Devices
Recall Status
ACTIVE

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